ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xp22.33(chrX:1790118-2761052)x3
Germline
Classification
(1)
Likely 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 | |||
CD99 |
|
- | - |
GRCh38 GRCh38 |
2 | 106 |
DHRSX | - | - |
GRCh38 GRCh38 |
8 | 133 | |
LINC00102 | - | - | - |
GRCh38 GRCh38 |
- | 106 |
MIR6089 | - | - | - |
GRCh38 GRCh38 |
- | 106 |
XG | - | - |
GRCh38 GRCh37 |
20 | 265 | |
ZBED1 | - | - |
GRCh38 GRCh38 |
- | 118 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jul 18, 2014 | RCV000142315.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024