ClinVar Genomic variation as it relates to human health
GRCh38/hg38 22q13.31-13.33(chr22:43807366-50739836)x1
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 | |||
SHANK3 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 GRCh37 |
824 | 1051 | |
ACR | - | - |
GRCh38 GRCh38 GRCh37 |
33 | 200 | |
ADM2 | - | - |
GRCh38 GRCh37 |
18 | 172 | |
ALG12 | - | - |
GRCh38 GRCh37 |
526 | 764 | |
ARHGAP8 | - | - |
GRCh38 GRCh37 |
- | 165 | |
ARSA | - | - |
GRCh38 GRCh37 |
1251 | 1419 | |
ATXN10 | - | - |
GRCh38 GRCh37 |
36 | 124 | |
BRD1 | - | - |
GRCh38 GRCh37 |
84 | 225 | |
CDPF1 | - | - | - |
GRCh38 GRCh37 |
9 | 95 |
CELSR1 | - | - |
GRCh38 GRCh37 |
489 | 638 |
There are 433 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 | RCV000051408.8 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024