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rs187075894

From SNPedia

Orientationplus
Stabilizedplus
Make rs187075894(C;C)
Make rs187075894(C;T)
Make rs187075894(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position12109925
is asnp
is mentioned by
dbSNPrs187075894
dbSNP (classic)rs187075894
ClinGenrs187075894
ebirs187075894
HLIrs187075894
Exacrs187075894
Gnomadrs187075894
Varsomers187075894
LitVarrs187075894
Maprs187075894
PheGenIrs187075894
Biobankrs187075894
1000 genomesrs187075894
hgdprs187075894
ensemblrs187075894
geneviewrs187075894
scholarrs187075894
googlers187075894
pharmgkbrs187075894
gwascentralrs187075894
openSNPrs187075894
23andMers187075894
SNPshotrs187075894
SNPdbers187075894
MSV3drs187075894
GWAS Ctlgrs187075894
GMAF0.09137
Max Magnitude0
GWAS snp
PMID [PMID 23319000]
Trait Metabolite levels (MHPG)
Title Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Risk Allele C
P-val 8E-7
Odds Ratio .31 unit increase