ClinVar Genomic variation as it relates to human health
GRCh37/hg19 15q25.2-25.3(chr15:85089553-85876582)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 | |||
ZNF592 | No evidence available | No evidence available |
GRCh38 GRCh37 |
103 | 157 | |
ALPK3 | - | - |
GRCh38 GRCh37 |
2292 | 2420 | |
NMB | - | - |
GRCh38 GRCh38 GRCh37 |
10 | 64 | |
PDE8A | - | - |
GRCh38 GRCh37 |
40 | 96 | |
SEC11A | - | - |
GRCh38 GRCh37 |
6 | 60 | |
SLC28A1 | - | - |
GRCh38 GRCh37 |
67 | 123 | |
WDR73 | - | - |
GRCh38 GRCh38 GRCh37 |
187 | 241 | |
ZSCAN2 | - | - | - |
GRCh38 GRCh38 GRCh37 |
39 | 112 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 2, 2022 | RCV001259717.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022