ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6q21(chr6:109796301-113083437)x3
Germline
Classification
(1)
Uncertain significance
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
AK9 | - | - |
GRCh38 GRCh37 |
83 | 139 | |
AMD1 | - | - |
GRCh38 GRCh37 |
7 | 41 | |
CCN6 | - | - |
GRCh38 GRCh37 |
221 | 246 | |
CDC40 | - | - |
GRCh38 GRCh37 |
16 | 43 | |
CDK19 | - | - |
GRCh38 GRCh37 |
39 | 73 | |
DDO | - | - |
GRCh38 GRCh37 |
29 | 56 | |
FAM229B | - | - | - |
GRCh38 GRCh37 |
8 | 34 |
FIG4 | - | - |
GRCh38 GRCh37 |
985 | 1023 | |
FYN | - | - |
GRCh38 GRCh37 |
28 | 52 | |
GPR6 | - | - |
GRCh38 GRCh37 |
23 | 49 |
There are 14 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Mar 25, 2021 | RCV001353182.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022