ClinVar Genomic variation as it relates to human health
GRCh37/hg19 13q32.1(chr13:96487525-97295519)x4
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 | |||
HS6ST3 | - | - |
GRCh38 GRCh37 |
40 | 133 | |
UGGT2 | - | - |
GRCh38 GRCh37 |
99 | 189 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 9, 2018 | RCV000683536.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022