ClinVar Genomic variation as it relates to human health
GRCh38/hg38 15q25.2-25.3(chr15:84391435-85157671)x1
Germline
Classification
(1)
Uncertain significance
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 | |||
ZNF592 | No evidence available | No evidence available |
GRCh38 GRCh37 |
103 | 157 | |
ALPK3 | - | - |
GRCh38 GRCh37 |
2292 | 2420 | |
LINC00933 | - | - | - |
GRCh38 GRCh38 |
- | 14 |
LOC103171574 | - | - | - |
GRCh38 GRCh38 GRCh38 |
- | 12 |
LOC105370947 | - | - | - |
GRCh38 GRCh38 |
- | 33 |
LOC111718493 | - | - | - | GRCh38 | - | 86 |
LOC125138300 | - | - | - | GRCh38 | - | 14 |
LOC130057801 | - | - | - |
GRCh38 GRCh38 |
- | 14 |
LOC130057802 | - | - | - |
GRCh38 GRCh38 |
- | 14 |
LOC130057803 | - | - | - |
GRCh38 GRCh38 |
- | 14 |
There are 33 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Apr 27, 2011 | RCV000137479.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024