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rs3795958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3795958(A;G)
Make rs3795958(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26444262
GeneDRC1
is asnp
is mentioned by
dbSNPrs3795958
dbSNP (classic)rs3795958
ClinGenrs3795958
ebirs3795958
HLIrs3795958
Exacrs3795958
Gnomadrs3795958
Varsomers3795958
LitVarrs3795958
Maprs3795958
PheGenIrs3795958
Biobankrs3795958
1000 genomesrs3795958
hgdprs3795958
ensemblrs3795958
geneviewrs3795958
scholarrs3795958
googlers3795958
pharmgkbrs3795958
gwascentralrs3795958
openSNPrs3795958
23andMers3795958
SNPshotrs3795958
SNPdbers3795958
MSV3drs3795958
GWAS Ctlgrs3795958
GMAF0.1584
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23319000]
Trait Metabolite levels (HVA)
Title Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Risk Allele G
P-val 2E-6
Odds Ratio .24 unit increase


ClinVar
Risk rs3795958(G;G)
Alt rs3795958(G;G)
Reference Rs3795958(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene DRC1
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.26667130A>G
CLNSRC
CLNACC RCV000454516.1,