ClinVar Genomic variation as it relates to human health
GRCh38/hg38 3q25.1(chr3:151182346-151437002)x3
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 | |||
GPR171 | - | - |
GRCh38 GRCh37 |
- | 44 | |
GPR87 | - | - |
GRCh38 GRCh37 |
- | 53 | |
IGSF10 | - | - |
GRCh38 GRCh37 |
414 | 443 | |
LOC123192019 | - | - | - | GRCh38 | - | 4 |
LOC123192020 | - | - | - | GRCh38 | - | 4 |
LOC123192021 | - | - | - | GRCh38 | - | 5 |
LOC126806846 | - | - | - | GRCh38 | - | 4 |
LOC129937768 | - | - | - | GRCh38 | - | 4 |
LOC129937769 | - | - | - | GRCh38 | - | 5 |
MED12L | - | - |
GRCh38 GRCh37 |
178 | 486 |
There are 3 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Apr 30, 2011 | RCV000141402.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023