ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19p12(chr19:23855084-24340741)x3
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
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 | |||
ZNF254 | - | - |
GRCh38 GRCh37 |
70 | 91 | |
ZNF675 | - | - |
GRCh38 GRCh37 |
36 | 66 | |
ZNF681 | - | - | - |
GRCh38 GRCh37 |
43 | 73 |
ZNF726 | - | - | - |
GRCh38 GRCh37 |
- | 25 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jun 1, 2018 | RCV000762781.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 24, 2022