ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xp11.4(chrX:37955473-38120350)x3
Germline
Classification
(1)
Likely benign
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 | |||
H2AL3 | - | - | - | GRCh38 | - | 74 |
H2AP | - | - | - |
GRCh38 GRCh37 |
- | 161 |
LOC130068096 | - | - | - | GRCh38 | - | 73 |
LOC130068097 | - | - | - | GRCh38 | - | 73 |
MIR548AJ2 | - | - | - | GRCh38 | - | 73 |
SYTL5 | - | - | - |
GRCh38 GRCh37 |
52 | 215 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Sep 21, 2012 | RCV000138478.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024