ClinVar Genomic variation as it relates to human health
NM_152721.6(DOK6):c.67-22582_67-14452del
Germline
Classification
(4)
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 | |||
DOK6 | - | - |
GRCh38 GRCh37 |
19 | 161 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161849.3 | |
not provided (1) |
|
- | RCV000161850.3 | |
not provided (1) |
|
- | RCV000161851.3 | |
not provided (1) |
|
- | RCV000161852.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Jun 23, 2024