ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xp22.33-22.2(chrX:251879-9798930)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 | |||
ANOS1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
279 | 509 | |
ARSL | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
422 | 661 | |
NLGN4X | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
257 | 476 | |
SHOX |
|
Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh38 |
155 | 351 |
STS | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
125 | 505 | |
VCX3A | No evidence available | Dosage sensitivity unlikely |
GRCh38 GRCh37 |
5 | 332 | |
ARSD | No evidence available | No evidence available |
GRCh38 GRCh37 |
61 | 301 | |
AKAP17A |
|
- | - |
GRCh38 GRCh38 |
- | 110 |
ARSD-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 232 |
ARSF | - | - |
GRCh38 GRCh37 |
53 | 287 |
There are 125 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) |
|
Jul 16, 2013 | RCV000141931.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024