ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xp11.22(chrX:51476578-53087050)x0
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 | |||
FAM156A | - | - | - |
GRCh38 GRCh37 |
- | 138 |
FAM156B | - | - | - |
GRCh38 GRCh37 |
- | 138 |
GPR173 | - | - |
GRCh38 GRCh37 |
10 | 151 | |
GSPT2 | - | - |
GRCh38 GRCh37 |
19 | 177 | |
MAGED1 | - | - |
GRCh38 GRCh37 |
40 | 195 | |
MAGED4 | - | - |
GRCh38 GRCh37 |
- | 154 | |
MAGED4B | - | - |
GRCh38 GRCh37 |
- | 154 | |
SPANXN5 | - | - |
GRCh38 GRCh37 |
5 | 144 | |
SSX2 | - | - |
GRCh38 GRCh37 |
- | 142 | |
SSX2B | - | - | - |
GRCh38 GRCh37 |
- | 141 |
There are 6 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 18, 2018 | RCV000848734.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022