rs2376805
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2376805(C;T) |
Make rs2376805(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 2024923 |
Gene | GABRD |
is a | snp |
is | mentioned by |
dbSNP | rs2376805 |
dbSNP (classic) | rs2376805 |
ClinGen | rs2376805 |
ebi | rs2376805 |
HLI | rs2376805 |
Exac | rs2376805 |
Gnomad | rs2376805 |
Varsome | rs2376805 |
LitVar | rs2376805 |
Map | rs2376805 |
PheGenI | rs2376805 |
Biobank | rs2376805 |
1000 genomes | rs2376805 |
hgdp | rs2376805 |
ensembl | rs2376805 |
geneview | rs2376805 |
scholar | rs2376805 |
rs2376805 | |
pharmgkb | rs2376805 |
gwascentral | rs2376805 |
openSNP | rs2376805 |
23andMe | rs2376805 |
SNPshot | rs2376805 |
SNPdbe | rs2376805 |
MSV3d | rs2376805 |
GWAS Ctlg | rs2376805 |
GMAF | 0.2011 |
Max Magnitude | 0 |
[PMID 20561060] Association of the GABRD gene and childhood-onset mood disorders
ClinVar | |
---|---|
Risk | rs2376805(T;T) |
Alt | rs2376805(T;T) |
Reference | Rs2376805(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | GABRD |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000001.10:g.1956362G>A |
CLNSRC | |
CLNACC | RCV000245842.1, |