ClinVar Genomic variation as it relates to human health
NR_125764.1(LINC01322):n.201-50931_201-19041del
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 | |||
LINC01322 | - | - | - | GRCh38 | 1 | 10 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161322.1 | |
not provided (1) |
|
- | RCV000161323.1 | |
not provided (1) |
|
- | RCV000161324.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022