ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.2-14.1(chr11:13970757-27565888)x3
Germline
Classification
(1)
Pathogenic
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 | |||
SOX6 | No evidence available | No evidence available |
GRCh38 GRCh37 |
154 | 186 | |
ABCC8 | - | - |
GRCh38 GRCh37 |
2335 | 2467 | |
ANO3 | - | - |
GRCh38 GRCh37 |
485 | 557 | |
ANO5 | - | - |
GRCh38 GRCh37 |
1288 | 1324 | |
BBOX1 | - | - |
GRCh38 GRCh37 |
- | 59 | |
BDNF-AS | - | - |
GRCh38 GRCh37 |
- | 95 | |
C11orf58 | - | - |
GRCh38 GRCh37 |
1 | 17 | |
CALCA | - | - |
GRCh38 GRCh37 |
12 | 31 | |
CALCB | - | - |
GRCh38 GRCh37 |
13 | 35 | |
CCDC179 | - | - | - |
GRCh38 GRCh37 |
- | 33 |
There are 59 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Apr 15, 2019 | RCV001006388.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024