ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q24.1-25(chr11:121611476-135068576)x1
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 | |||
CHEK1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
65 | 148 | |
ACAD8 | - | - |
GRCh38 GRCh37 |
259 | 360 | |
ACRV1 | - | - |
GRCh38 GRCh37 |
- | 72 | |
ADAMTS15 | - | - |
GRCh38 GRCh37 |
72 | 153 | |
ADAMTS8 | - | - |
GRCh38 GRCh37 |
62 | 143 | |
APLP2 | - | - |
GRCh38 GRCh37 |
58 | 136 | |
ARHGAP32 | - | - |
GRCh38 GRCh37 |
155 | 242 | |
B3GAT1 | - | - |
GRCh38 GRCh37 |
14 | 111 | |
B3GAT1-DT | - | - | - | GRCh38 | 1 | 48 |
BARX2 | - | - |
GRCh38 GRCh37 |
17 | 93 |
There are 436 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Nov 19, 2013 | RCV000142185.7 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024