ClinVar Genomic variation as it relates to human health
GRCh37/hg19 6p25.3(chr6:951385-1832936)x3
Germline
Classification
(1)
Pathogenic
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 | |||
FOXC1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
533 | 674 | |
FOXF2 | - | - |
GRCh38 GRCh37 |
10 | 122 | |
FOXQ1 | - | - |
GRCh38 GRCh37 |
66 | 138 | |
GMDS | - | - |
GRCh38 GRCh37 |
29 | 122 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jun 9, 2015 | RCV000416532.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jul 19, 2022