ClinVar Genomic variation as it relates to human health
GRCh37/hg19 9q34.2(chr9:136850292-137153876)
Germline
Classification
(1)
Likely benign
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 | |||
BRD3 | - | - |
GRCh38 GRCh37 |
36 | 74 | |
RNU6ATAC | - | - |
GRCh38 GRCh37 |
- | 39 | |
VAV2 | - | - |
GRCh38 GRCh37 |
62 | 101 | |
WDR5 | - | - |
GRCh38 GRCh37 |
13 | 52 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Dec 15, 2015 | RCV000416829.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022