ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.41(chr19:53057478-53428612)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 | |||
ZNF28 | - | - | - |
GRCh38 GRCh37 |
- | 77 |
ZNF320 | - | - |
GRCh38 GRCh37 |
26 | 45 | |
ZNF468 | - | - |
GRCh38 GRCh37 |
41 | 62 | |
ZNF600 | - | - | - |
GRCh38 GRCh37 |
77 | 154 |
ZNF611 | - | - | - |
GRCh38 GRCh37 |
64 | 83 |
ZNF701 | - | - | - |
GRCh38 GRCh37 |
50 | 66 |
ZNF808 | - | - | - |
GRCh38 GRCh37 |
78 | 96 |
ZNF83 | - | - |
GRCh38 GRCh37 |
29 | 57 | |
ZNF888 | - | - | - |
GRCh38 GRCh37 |
2 | 20 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Oct 28, 2019 | RCV001259945.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022