ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3p25.1(chr3:15648003-16355532)x3
Germline
Classification
(1)
Likely benign
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 | |||
ANKRD28 | - | - |
GRCh38 GRCh37 |
12 | 84 | |
BTD | - | - |
GRCh38 GRCh37 |
659 | 736 | |
DPH3 | - | - |
GRCh38 GRCh37 |
1 | 27 | |
GALNT15 | - | - |
GRCh38 GRCh37 |
61 | 87 | |
OXNAD1 | - | - | - |
GRCh38 GRCh37 |
20 | 58 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Mar 28, 2018 | RCV000682248.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023