ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10p15.1(chr10:4504067-5395279)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 | |||
AKR1C1 | - | - |
GRCh38 GRCh37 |
31 | 72 | |
AKR1C2 | - | - |
GRCh38 GRCh37 |
82 | 131 | |
AKR1C3 | - | - |
GRCh38 GRCh37 |
30 | 72 | |
AKR1C4 | - | - |
GRCh38 GRCh37 |
69 | 106 | |
AKR1E2 | - | - |
GRCh38 GRCh37 |
122 | 160 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jan 26, 2019 | RCV001006290.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022