ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p15.3-13(chr11:11053978-34732891)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 | |||
PAX6 | Sufficient evidence for dosage pathogenicity | Little evidence for dosage pathogenicity |
GRCh38 GRCh37 |
668 | 870 | |
WT1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
896 | 1644 | |
SOX6 | No evidence available | No evidence available |
GRCh38 GRCh37 |
144 | 173 | |
ABCC8 | - | - |
GRCh38 GRCh37 |
2308 | 2434 | |
ABTB2 | - | - | - |
GRCh38 GRCh37 |
75 | 99 |
ANO3 | - | - |
GRCh38 GRCh37 |
481 | 551 | |
ANO5 | - | - |
GRCh38 GRCh37 |
1274 | 1309 | |
ARL14EP | - | - |
GRCh38 GRCh37 |
11 | 31 | |
BBOX1 | - | - |
GRCh38 GRCh37 |
- | 57 | |
BDNF | - | - |
GRCh38 GRCh37 |
7 | 97 |
There are 108 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) |
|
Sep 18, 2018 | RCV001006387.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 01, 2024