ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xq26.2(chrX:131885089-132500236)x2
Germline
Classification
(1)
Uncertain significance
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 | |||
GPC4 | - | - |
GRCh38 GRCh37 |
76 | 254 | |
HS6ST2 | - | - |
GRCh38 GRCh37 |
52 | 234 | |
TFDP3 | - | - |
GRCh38 GRCh37 |
16 | 193 | |
USP26 | - | - |
GRCh38 GRCh37 |
58 | 233 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Jul 6, 2015 | RCV000203429.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 30, 2023