ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.12(chr19:37325796-37516374)x1
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 | |||
ZNF345 | - | - | - |
GRCh38 GRCh37 |
12 | 70 |
ZNF568 | - | - |
GRCh38 GRCh37 |
39 | 57 | |
ZNF790 | - | - | - |
GRCh38 GRCh37 |
- | 59 |
ZNF829 | - | - | - |
GRCh38 GRCh37 |
12 | 47 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 27, 2019 | RCV001007044.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022