ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11q23.3-25(chr11:118789765-134998513)x3
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
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 | |||
HMBS | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
589 | 635 | |
CBL | No evidence available | No evidence available |
GRCh38 GRCh37 |
1450 | 1604 | |
CHEK1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
71 | 155 | |
ABCG4 | - | - |
GRCh38 GRCh37 |
23 | 61 | |
ACAD8 | - | - |
GRCh38 GRCh37 |
260 | 361 | |
ACRV1 | - | - |
GRCh38 GRCh37 |
- | 72 | |
ADAMTS15 | - | - |
GRCh38 GRCh37 |
79 | 160 | |
ADAMTS8 | - | - |
GRCh38 GRCh37 |
65 | 146 | |
APLP2 | - | - |
GRCh38 GRCh37 |
68 | 146 | |
ARHGAP32 | - | - |
GRCh38 GRCh37 |
172 | 259 |
There are 627 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 |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Aug 12, 2011 | RCV000051213.8 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024