ClinVar Genomic variation as it relates to human health
NM_003396.3(WNT9B):c.335-7G>C
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 | |||
LRRC37A2 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
- | 642 | |
WNT9B | - | - |
GRCh38 GRCh38 GRCh37 |
- | 76 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
WNT9B-related disorder
|
Likely benign (1) |
|
Sep 19, 2019 | RCV003926782.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024