ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3p22.2(chr3:37309935-37523143)x1
Germline
Classification
(1)
Uncertain significance
no assertion criteria 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 | |||
APRG1 | - | - |
GRCh38 GRCh38 GRCh37 |
2 | 22 | |
GOLGA4 | - | - |
GRCh38 GRCh37 |
135 | 165 | |
ITGA9 | - | - |
GRCh38 GRCh38 GRCh37 |
88 | 123 | |
LOC129389056 | - | - | - | GRCh38 | - | 8 |
LOC129936472 | - | - | - |
GRCh38 GRCh38 |
- | 4 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
May 14, 2013 | RCV000141777.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024