ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xp21.1(chrX:34645143-35206581)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 | |||
FAM47B | - | - | - |
GRCh38 GRCh37 |
61 | 212 |
TMEM47 | - | - |
GRCh38 GRCh37 |
6 | 158 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
May 17, 2019 | RCV001007293.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022