ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xq26.3(chrX:135591295-135741703)x2
Germline
Classification
(1)
Benign
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 | |||
CT45A1 | - | - |
GRCh38 GRCh37 |
1 | 175 | |
LOC126863324 | - | - | - | GRCh38 | - | 85 |
LOC130068742 | - | - | - | GRCh38 | - | 84 |
LOC130068743 | - | - | - | GRCh38 | - | 84 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Oct 19, 2010 | RCV000137017.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024