ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17p13.1(chr17:7937691-8247776)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 | |||
ALOX12B | - | - |
GRCh38 GRCh37 |
307 | 364 | |
ALOX15B | - | - |
GRCh38 GRCh37 |
62 | 95 | |
ALOXE3 | - | - |
GRCh38 GRCh37 |
215 | 294 | |
ARHGEF15 | - | - |
GRCh38 GRCh37 |
589 | 617 | |
AURKB | - | - |
GRCh38 GRCh37 |
20 | 49 | |
BORCS6 | - | - |
GRCh38 GRCh37 |
26 | 56 | |
CTC1 | - | - |
GRCh38 GRCh37 |
1366 | 1482 | |
HES7 | - | - |
GRCh38 GRCh37 |
69 | 150 | |
ODF4 | - | - |
GRCh38 GRCh37 |
11 | 37 | |
PER1 | - | - |
GRCh38 GRCh37 |
107 | 139 |
There are 10 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 15, 2019 | RCV001006868.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022