ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xq28(chrX:150912962-151423949)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 | |||
CNGA2 | - | - |
GRCh38 GRCh37 |
63 | 247 | |
GABRA3 | - | - |
GRCh38 GRCh37 |
35 | 226 | |
GABRE | - | - |
GRCh38 GRCh37 |
52 | 239 | |
MAGEA10 | - | - |
GRCh38 GRCh37 |
- | 209 | |
MAGEA4 | - | - |
GRCh38 GRCh37 |
33 | 219 | |
MIR224 | - | - |
GRCh38 GRCh37 |
- | 186 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 3, 2023 | RCV003483982.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 04, 2024