ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xq22.1(chrX:99858343-100348232)x3
Germline
Classification
(1)
Uncertain significance
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 | |||
SRPX2 | No evidence available | No evidence available |
GRCh38 GRCh37 |
166 | 341 | |
ARL13A | - | - | - |
GRCh38 GRCh37 |
- | 171 |
CSTF2 | - | - |
GRCh38 GRCh37 |
19 | 190 | |
NOX1 | - | - |
GRCh38 GRCh37 |
46 | 219 | |
SYTL4 | - | - |
GRCh38 GRCh37 |
29 | 202 | |
TMEM35A | - | - | - |
GRCh38 GRCh37 |
2 | 170 |
TRMT2B | - | - | - |
GRCh38 GRCh37 |
14 | 185 |
TSPAN6 | - | - |
GRCh38 GRCh37 |
9 | 178 | |
XKRX | - | - |
GRCh38 GRCh37 |
18 | 193 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 19, 2020 | RCV001259486.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022