ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q23.1(chr10:83476233-86036350)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 | |||
NRG3 | No evidence available | No evidence available |
GRCh38 GRCh37 |
77 | 120 | |
CDHR1 | - | - |
GRCh38 GRCh37 |
901 | 952 | |
GHITM | - | - |
GRCh38 GRCh37 |
26 | 72 | |
GPR15LG | - | - |
GRCh38 GRCh37 |
- | 43 | |
LRIT1 | - | - |
GRCh38 GRCh37 |
67 | 114 | |
LRIT2 | - | - | - |
GRCh38 GRCh37 |
42 | 91 |
RGR | - | - |
GRCh38 GRCh37 |
284 | 331 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Jun 23, 2014 | RCV000510200.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024