ClinVar Genomic variation as it relates to human health
NM_000762.5(CYP2A6):c.-22817_-420del
Germline
Classification
(3)
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 | |||
LOC110673974 | - | - | - | GRCh38 | 1 | 6 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161870.2 | |
not provided (1) |
|
- | RCV000161871.2 | |
not provided (1) |
|
- | RCV000161869.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024