ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q25.3(chr10:115274398-115542099)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 | |||
CASP7 | - | - |
GRCh38 GRCh37 |
21 | 57 | |
HABP2 | - | - |
GRCh38 GRCh37 |
193 | 262 | |
NRAP | - | - |
GRCh38 GRCh37 |
240 | 305 | |
PLEKHS1 | - | - | - |
GRCh38 GRCh37 |
42 | 72 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
- | RCV000447230.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024