ClinVar Genomic variation as it relates to human health
NM_001010848.3(NRG3):c.824-173790_824-159316del
Germline
Classification
(2)
not provided
no classification 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 | |||
NRG3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
77 | 120 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161606.3 | |
not provided (1) |
|
- | RCV000161607.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 23, 2024