ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q21.3(chr10:66318723-66354723)x1
Germline
Classification
(4)
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 | |||
CTNNA3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
958 | 1027 | |
LOC132089819 | - | - | - | GRCh38 | - | 15 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
not provided (1) |
|
- | RCV000161596.2 | |
not provided (1) |
|
- | RCV000161597.2 | |
not provided (1) |
|
- | RCV000161599.2 | |
Benign (1) |
|
Jan 7, 2015 | RCV000225157.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024