ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Xp22.2(chrX:14878636-14942042)
Germline
Classification
(1)
Pathogenic
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 | |||
FANCB | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
628 | 818 | |
MOSPD2 | - | - |
GRCh38 GRCh37 |
15 | 185 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Mar 1, 2022 | RCV002052780.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022