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rs2376805

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2376805(C;T)
Make rs2376805(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position2024923
GeneGABRD
is asnp
is mentioned by
dbSNPrs2376805
ebirs2376805
HLIrs2376805
Exacrs2376805
Varsomers2376805
Maprs2376805
PheGenIrs2376805
hapmaprs2376805
1000 genomesrs2376805
hgdprs2376805
ensemblrs2376805
gopubmedrs2376805
geneviewrs2376805
scholarrs2376805
googlers2376805
pharmgkbrs2376805
gwascentralrs2376805
openSNPrs2376805
23andMers2376805
23andMe allrs2376805
SNP Nexus

SNPshotrs2376805
SNPdbers2376805
MSV3drs2376805
GWAS Ctlgrs2376805
GMAF0.2011
Max Magnitude0

[PMID 20561060OA-icon.png] 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,