ClinVar Genomic variation as it relates to human health
GRCh37/hg19 22q11.23(chr22:24328565-24385948)x0
Germline
Classification
(1)
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 | |||
GSTT1 | - | - |
GRCh38 GRCh37 |
5 | 74 | |
GSTT1-AS1 | - | - | - | GRCh38 | - | 3 |
GSTT4 | - | - | - |
GRCh38 GRCh38 |
1 | 44 |
LOC391322 | - | - | - | GRCh38 | 3 | 6 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Benign (1) |
|
Mar 8, 2011 | RCV000136388.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024