Name: rs10844844
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs10844844

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:34227415 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: C>A
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.257649 (68197/264690, TOPMED)
A=0.353857 (63869/180494, ALFA)
A=0.278594 (39011/140028, GnomAD) (+ 21 more)
A=0.16319 (12843/78700, PAGE_STUDY)
A=0.00549 (155/28258, 14KJPN)
A=0.00537 (90/16760, 8.3KJPN)
A=0.1711 (1096/6404, 1000G_30x)
A=0.1717 (860/5008, 1000G)
A=0.3801 (1465/3854, ALSPAC)
A=0.3970 (1472/3708, TWINSUK)
A=0.0103 (30/2922, KOREAN)
A=0.2123 (442/2082, HGDP_Stanford)
A=0.1494 (280/1874, HapMap)
A=0.0098 (18/1832, Korea1K)
A=0.378 (377/998, GoNL)
A=0.021 (17/792, PRJEB37584)
A=0.286 (179/626, Chileans)
A=0.383 (230/600, NorthernSweden)
A=0.264 (57/216, Qatari)
A=0.019 (4/214, Vietnamese)
C=0.419 (67/160, SGDP_PRJ)
A=0.35 (14/40, GENOME_DK)
C=0.42 (15/36, Siberian)
A=0.10 (2/20, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	185530	C=0.647739	A=0.352261
European	Sub	159636	C=0.621683	A=0.378317
African	Sub	7620	C=0.9059	A=0.0941
African Others	Sub	290	C=0.934	A=0.066
African American	Sub	7330	C=0.9048	A=0.0952
Asian	Sub	3478	C=0.9899	A=0.0101
East Asian	Sub	2804	C=0.9904	A=0.0096
Other Asian	Sub	674	C=0.988	A=0.012
Latin American 1	Sub	686	C=0.706	A=0.294
Latin American 2	Sub	3676	C=0.7089	A=0.2911
South Asian	Sub	5150	C=0.7012	A=0.2988
Other	Sub	5284	C=0.7352	A=0.2648

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	C=0.742351	A=0.257649
Allele Frequency Aggregator	Total	Global	180494	C=0.646143	A=0.353857
Allele Frequency Aggregator	European	Sub	156542	C=0.621616	A=0.378384
Allele Frequency Aggregator	African	Sub	6478	C=0.9072	A=0.0928
Allele Frequency Aggregator	South Asian	Sub	5150	C=0.7012	A=0.2988
Allele Frequency Aggregator	Other	Sub	4484	C=0.7348	A=0.2652
Allele Frequency Aggregator	Latin American 2	Sub	3676	C=0.7089	A=0.2911
Allele Frequency Aggregator	Asian	Sub	3478	C=0.9899	A=0.0101
Allele Frequency Aggregator	Latin American 1	Sub	686	C=0.706	A=0.294
gnomAD - Genomes	Global	Study-wide	140028	C=0.721406	A=0.278594
gnomAD - Genomes	European	Sub	75830	C=0.60819	A=0.39181
gnomAD - Genomes	African	Sub	41964	C=0.90542	A=0.09458
gnomAD - Genomes	American	Sub	13628	C=0.72791	A=0.27209
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	C=0.6992	A=0.3008
gnomAD - Genomes	East Asian	Sub	3134	C=0.9876	A=0.0124
gnomAD - Genomes	Other	Sub	2148	C=0.7281	A=0.2719
The PAGE Study	Global	Study-wide	78700	C=0.83681	A=0.16319
The PAGE Study	AfricanAmerican	Sub	32514	C=0.89552	A=0.10448
The PAGE Study	Mexican	Sub	10810	C=0.70675	A=0.29325
The PAGE Study	Asian	Sub	8318	C=0.9911	A=0.0089
The PAGE Study	PuertoRican	Sub	7918	C=0.7767	A=0.2233
The PAGE Study	NativeHawaiian	Sub	4534	C=0.8871	A=0.1129
The PAGE Study	Cuban	Sub	4230	C=0.7201	A=0.2799
The PAGE Study	Dominican	Sub	3828	C=0.7675	A=0.2325
The PAGE Study	CentralAmerican	Sub	2450	C=0.7310	A=0.2690
The PAGE Study	SouthAmerican	Sub	1982	C=0.7296	A=0.2704
The PAGE Study	NativeAmerican	Sub	1260	C=0.6643	A=0.3357
The PAGE Study	SouthAsian	Sub	856	C=0.731	A=0.269
14KJPN	JAPANESE	Study-wide	28258	C=0.99451	A=0.00549
8.3KJPN	JAPANESE	Study-wide	16760	C=0.99463	A=0.00537
1000Genomes_30x	Global	Study-wide	6404	C=0.8289	A=0.1711
1000Genomes_30x	African	Sub	1786	C=0.9642	A=0.0358
1000Genomes_30x	Europe	Sub	1266	C=0.6066	A=0.3934
1000Genomes_30x	South Asian	Sub	1202	C=0.7579	A=0.2421
1000Genomes_30x	East Asian	Sub	1170	C=0.9863	A=0.0137
1000Genomes_30x	American	Sub	980	C=0.768	A=0.232
1000Genomes	Global	Study-wide	5008	C=0.8283	A=0.1717
1000Genomes	African	Sub	1322	C=0.9592	A=0.0408
1000Genomes	East Asian	Sub	1008	C=0.9851	A=0.0149
1000Genomes	Europe	Sub	1006	C=0.6093	A=0.3907
1000Genomes	South Asian	Sub	978	C=0.754	A=0.246
1000Genomes	American	Sub	694	C=0.774	A=0.226
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.6199	A=0.3801
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.6030	A=0.3970
KOREAN population from KRGDB	KOREAN	Study-wide	2922	C=0.9897	A=0.0103
HGDP-CEPH-db Supplement 1	Global	Study-wide	2082	C=0.7877	A=0.2123
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.957	A=0.043
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.732	A=0.268
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.617	A=0.383
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.625	A=0.375
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.950	A=0.050
HGDP-CEPH-db Supplement 1	America	Sub	214	C=0.790	A=0.210
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=1.00	A=0.00
HapMap	Global	Study-wide	1874	C=0.8506	A=0.1494
HapMap	American	Sub	760	C=0.739	A=0.261
HapMap	African	Sub	684	C=0.966	A=0.034
HapMap	Asian	Sub	254	C=0.984	A=0.016
HapMap	Europe	Sub	176	C=0.688	A=0.312
Korean Genome Project	KOREAN	Study-wide	1832	C=0.9902	A=0.0098
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.622	A=0.378
CNV burdens in cranial meningiomas	Global	Study-wide	792	C=0.979	A=0.021
CNV burdens in cranial meningiomas	CRM	Sub	792	C=0.979	A=0.021
Chileans	Chilean	Study-wide	626	C=0.714	A=0.286
Northern Sweden	ACPOP	Study-wide	600	C=0.617	A=0.383
Qatari	Global	Study-wide	216	C=0.736	A=0.264
A Vietnamese Genetic Variation Database	Global	Study-wide	214	C=0.981	A=0.019
SGDP_PRJ	Global	Study-wide	160	C=0.419	A=0.581
The Danish reference pan genome	Danish	Study-wide	40	C=0.65	A=0.35
Siberian	Global	Study-wide	36	C=0.42	A=0.58
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	20	C=0.90	A=0.10

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 12	NC_000012.12:g.34227415C>A
GRCh37.p13 chr 12	NC_000012.11:g.34380350C>A

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	C=	A
GRCh38.p14 chr 12	NC_000012.12:g.34227415=	NC_000012.12:g.34227415C>A
GRCh37.p13 chr 12	NC_000012.11:g.34380350=	NC_000012.11:g.34380350C>A

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

100 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_SNP	ss15923490	Feb 27, 2004 (120)
2	CSHL-HAPMAP	ss16593044	Feb 27, 2004 (120)
3	SC_SNP	ss18994467	Feb 27, 2004 (120)
4	SSAHASNP	ss20875734	Apr 05, 2004 (123)
5	PERLEGEN	ss24354157	Sep 20, 2004 (124)
6	ABI	ss40151797	Mar 13, 2006 (126)
7	AFFY	ss66503410	Nov 29, 2006 (127)
8	ILLUMINA	ss66666996	Nov 29, 2006 (127)
9	ILLUMINA	ss66904468	Nov 29, 2006 (127)
10	ILLUMINA	ss67027790	Nov 29, 2006 (127)
11	ILLUMINA	ss70381730	May 16, 2007 (127)
12	ILLUMINA	ss70501955	May 25, 2008 (130)
13	ILLUMINA	ss71028010	May 16, 2007 (127)
14	ILLUMINA	ss75570245	Dec 06, 2007 (129)
15	AFFY	ss76326457	Dec 08, 2007 (130)
16	KRIBB_YJKIM	ss85013135	Dec 15, 2007 (130)
17	HUMANGENOME_JCVI	ss97301297	Feb 05, 2009 (130)
18	1000GENOMES	ss111781898	Jan 25, 2009 (130)
19	ILLUMINA	ss121400328	Dec 01, 2009 (131)
20	ENSEMBL	ss132114802	Dec 01, 2009 (131)
21	ILLUMINA	ss152845199	Dec 01, 2009 (131)
22	ILLUMINA	ss159147004	Dec 01, 2009 (131)
23	COMPLETE_GENOMICS	ss168124625	Jul 04, 2010 (132)
24	ILLUMINA	ss169661170	Jul 04, 2010 (132)
25	ILLUMINA	ss170631150	Jul 04, 2010 (132)
26	AFFY	ss173269758	Jul 04, 2010 (132)
27	BCM-HGSC-SUB	ss208155483	Jul 04, 2010 (132)
28	1000GENOMES	ss235895268	Jul 15, 2010 (132)
29	1000GENOMES	ss242460354	Jul 15, 2010 (132)
30	GMI	ss286540677	Apr 25, 2013 (138)
31	PJP	ss291420045	May 09, 2011 (134)
32	ILLUMINA	ss536642707	Sep 08, 2015 (146)
33	SSMP	ss658645299	Apr 25, 2013 (138)
34	ILLUMINA	ss825351284	Jul 19, 2016 (147)
35	ILLUMINA	ss832659633	Jul 13, 2019 (153)
36	EVA-GONL	ss989420881	Aug 21, 2014 (142)
37	JMKIDD_LAB	ss1078382229	Aug 21, 2014 (142)
38	1000GENOMES	ss1344575565	Aug 21, 2014 (142)
39	DDI	ss1426900399	Apr 01, 2015 (144)
40	EVA_GENOME_DK	ss1576220102	Apr 01, 2015 (144)
41	EVA_DECODE	ss1599095763	Apr 01, 2015 (144)
42	EVA_UK10K_ALSPAC	ss1628365686	Apr 01, 2015 (144)
43	EVA_UK10K_TWINSUK	ss1671359719	Apr 01, 2015 (144)
44	EVA_SVP	ss1713320710	Apr 01, 2015 (144)
45	WEILL_CORNELL_DGM	ss1932784013	Feb 12, 2016 (147)
46	ILLUMINA	ss1946336000	Feb 12, 2016 (147)
47	ILLUMINA	ss1959427275	Feb 12, 2016 (147)
48	GENOMED	ss1967567428	Jul 19, 2016 (147)
49	JJLAB	ss2027143916	Sep 14, 2016 (149)
50	USC_VALOUEV	ss2155471558	Dec 20, 2016 (150)
51	GRF	ss2699806529	Nov 08, 2017 (151)
52	ILLUMINA	ss2710759088	Nov 08, 2017 (151)
53	GNOMAD	ss2909223653	Nov 08, 2017 (151)
54	SWEGEN	ss3009489119	Nov 08, 2017 (151)
55	ILLUMINA	ss3021421773	Nov 08, 2017 (151)
56	BIOINF_KMB_FNS_UNIBA	ss3027381266	Nov 08, 2017 (151)
57	CSHL	ss3350012196	Nov 08, 2017 (151)
58	ILLUMINA	ss3625620355	Oct 12, 2018 (152)
59	ILLUMINA	ss3626855409	Oct 12, 2018 (152)
60	ILLUMINA	ss3637957411	Oct 12, 2018 (152)
61	ILLUMINA	ss3638992908	Oct 12, 2018 (152)
62	ILLUMINA	ss3639498429	Oct 12, 2018 (152)
63	ILLUMINA	ss3642951533	Oct 12, 2018 (152)
64	ILLUMINA	ss3644588975	Oct 12, 2018 (152)
65	URBANLAB	ss3649811389	Oct 12, 2018 (152)
66	ILLUMINA	ss3651796418	Oct 12, 2018 (152)
67	EVA_DECODE	ss3693449929	Jul 13, 2019 (153)
68	ILLUMINA	ss3725317105	Jul 13, 2019 (153)
69	ACPOP	ss3738926823	Jul 13, 2019 (153)
70	ILLUMINA	ss3744097965	Jul 13, 2019 (153)
71	EVA	ss3750347339	Jul 13, 2019 (153)
72	PAGE_CC	ss3771685050	Jul 13, 2019 (153)
73	KHV_HUMAN_GENOMES	ss3815670880	Jul 13, 2019 (153)
74	EVA	ss3833070490	Apr 26, 2020 (154)
75	EVA	ss3840104339	Apr 26, 2020 (154)
76	EVA	ss3845588751	Apr 26, 2020 (154)
77	HGDP	ss3847447899	Apr 26, 2020 (154)
78	SGDP_PRJ	ss3878044504	Apr 26, 2020 (154)
79	KRGDB	ss3926597670	Apr 26, 2020 (154)
80	KOGIC	ss3971596273	Apr 26, 2020 (154)
81	EVA	ss3984665350	Apr 26, 2021 (155)
82	EVA	ss3985585770	Apr 26, 2021 (155)
83	EVA	ss4017583742	Apr 26, 2021 (155)
84	TOPMED	ss4914434464	Apr 26, 2021 (155)
85	TOMMO_GENOMICS	ss5205822094	Apr 26, 2021 (155)
86	EVA	ss5237509975	Apr 26, 2021 (155)
87	1000G_HIGH_COVERAGE	ss5290391607	Oct 13, 2022 (156)
88	HUGCELL_USP	ss5485216660	Oct 13, 2022 (156)
89	EVA	ss5510659694	Oct 13, 2022 (156)
90	1000G_HIGH_COVERAGE	ss5587608257	Oct 13, 2022 (156)
91	SANFORD_IMAGENETICS	ss5624299302	Oct 13, 2022 (156)
92	SANFORD_IMAGENETICS	ss5652931444	Oct 13, 2022 (156)
93	TOMMO_GENOMICS	ss5754834735	Oct 13, 2022 (156)
94	YY_MCH	ss5813165781	Oct 13, 2022 (156)
95	EVA	ss5837822129	Oct 13, 2022 (156)
96	EVA	ss5847407482	Oct 13, 2022 (156)
97	EVA	ss5847666046	Oct 13, 2022 (156)
98	EVA	ss5903943442	Oct 13, 2022 (156)
99	EVA	ss5944289137	Oct 13, 2022 (156)
100	EVA	ss5979388105	Oct 13, 2022 (156)
101	1000Genomes	NC_000012.11 - 34380350	Oct 12, 2018 (152)
102	1000Genomes_30x	NC_000012.12 - 34227415	Oct 13, 2022 (156)
103	The Avon Longitudinal Study of Parents and Children	NC_000012.11 - 34380350	Oct 12, 2018 (152)
104	Chileans	NC_000012.11 - 34380350	Apr 26, 2020 (154)
105	The Danish reference pan genome	NC_000012.11 - 34380350	Apr 26, 2020 (154)
106	gnomAD - Genomes	NC_000012.12 - 34227415	Apr 26, 2021 (155)
107	Genome of the Netherlands Release 5	NC_000012.11 - 34380350	Apr 26, 2020 (154)
108	HGDP-CEPH-db Supplement 1	NC_000012.10 - 34271617	Apr 26, 2020 (154)
109	HapMap	NC_000012.12 - 34227415	Apr 26, 2020 (154)
110	KOREAN population from KRGDB	NC_000012.11 - 34380350	Apr 26, 2020 (154)
111	Korean Genome Project	NC_000012.12 - 34227415	Apr 26, 2020 (154)
112	Northern Sweden	NC_000012.11 - 34380350	Jul 13, 2019 (153)
113	The PAGE Study	NC_000012.12 - 34227415	Jul 13, 2019 (153)
114	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000012.11 - 34380350	Apr 26, 2021 (155)
115	CNV burdens in cranial meningiomas	NC_000012.11 - 34380350	Apr 26, 2021 (155)
116	Qatari	NC_000012.11 - 34380350	Apr 26, 2020 (154)
117	SGDP_PRJ	NC_000012.11 - 34380350	Apr 26, 2020 (154)
118	Siberian	NC_000012.11 - 34380350	Apr 26, 2020 (154)
119	8.3KJPN	NC_000012.11 - 34380350	Apr 26, 2021 (155)
120	14KJPN	NC_000012.12 - 34227415	Oct 13, 2022 (156)
121	TopMed	NC_000012.12 - 34227415	Apr 26, 2021 (155)
122	UK 10K study - Twins	NC_000012.11 - 34380350	Oct 12, 2018 (152)
123	A Vietnamese Genetic Variation Database	NC_000012.11 - 34380350	Jul 13, 2019 (153)
124	ALFA	NC_000012.12 - 34227415	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs12811536	Sep 24, 2004 (123)
rs17513280	Dec 02, 2004 (124)
rs56441151	May 25, 2008 (130)
rs59121938	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3638992908, ss3639498429	NC_000012.9:34271616:C:A	NC_000012.12:34227414:C:A	(self)
125791, ss111781898, ss168124625, ss208155483, ss286540677, ss291420045, ss825351284, ss1599095763, ss1713320710, ss3642951533, ss3847447899	NC_000012.10:34271616:C:A	NC_000012.12:34227414:C:A	(self)
57309244, 31828061, 97062, 2920739, 14204378, 33775064, 12211688, 811697, 214842, 14825943, 30061484, 7987912, 63791401, 31828061, 7065411, ss235895268, ss242460354, ss536642707, ss658645299, ss832659633, ss989420881, ss1078382229, ss1344575565, ss1426900399, ss1576220102, ss1628365686, ss1671359719, ss1932784013, ss1946336000, ss1959427275, ss1967567428, ss2027143916, ss2155471558, ss2699806529, ss2710759088, ss2909223653, ss3009489119, ss3021421773, ss3350012196, ss3625620355, ss3626855409, ss3637957411, ss3644588975, ss3651796418, ss3738926823, ss3744097965, ss3750347339, ss3833070490, ss3840104339, ss3878044504, ss3926597670, ss3984665350, ss3985585770, ss4017583742, ss5205822094, ss5237509975, ss5510659694, ss5624299302, ss5652931444, ss5837822129, ss5847407482, ss5847666046, ss5944289137, ss5979388105	NC_000012.11:34380349:C:A	NC_000012.12:34227414:C:A	(self)
75134192, 404056080, 793996, 27974274, 906519, 88671839, 129980121, 6234779536, ss3027381266, ss3649811389, ss3693449929, ss3725317105, ss3771685050, ss3815670880, ss3845588751, ss3971596273, ss4914434464, ss5290391607, ss5485216660, ss5587608257, ss5754834735, ss5813165781, ss5903943442	NC_000012.12:34227414:C:A	NC_000012.12:34227414:C:A	(self)
ss15923490, ss16593044, ss18994467, ss20875734	NT_009714.16:27139323:C:A	NC_000012.12:34227414:C:A	(self)
ss24354157, ss40151797, ss66503410, ss66666996, ss66904468, ss67027790, ss70381730, ss70501955, ss71028010, ss75570245, ss76326457, ss85013135, ss97301297, ss121400328, ss132114802, ss152845199, ss159147004, ss169661170, ss170631150, ss173269758	NT_009714.17:27140473:C:A	NC_000012.12:34227414:C:A	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs10844844

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs10844844