ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xq21.1(chrX:77544318-78390511)x3
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 | |||
CYSLTR1 | - | - |
GRCh38 GRCh37 |
23 | 165 | |
LPAR4 | - | - |
GRCh38 GRCh37 |
18 | 151 | |
P2RY10 | - | - |
GRCh38 GRCh37 |
12 | 144 | |
RTL3 | - | - | - |
GRCh38 GRCh37 |
36 | 170 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 13, 2021 | RCV002475599.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022