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rs12134663

From SNPedia

Orientationplus
Stabilizedplus
Make rs12134663(A;A)
Make rs12134663(A;C)
Make rs12134663(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position11778589
GeneLOC100506310
is asnp
is mentioned by
dbSNPrs12134663
ebirs12134663
HLIrs12134663
Exacrs12134663
Varsomers12134663
Maprs12134663
PheGenIrs12134663
hapmaprs12134663
1000 genomesrs12134663
hgdprs12134663
ensemblrs12134663
gopubmedrs12134663
geneviewrs12134663
scholarrs12134663
googlers12134663
pharmgkbrs12134663
gwascentralrs12134663
openSNPrs12134663
23andMers12134663
23andMe allrs12134663
SNP Nexus

SNPshotrs12134663
SNPdbers12134663
MSV3drs12134663
GWAS Ctlgrs12134663
GMAF0.1134
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23824729OA-icon.png]
Trait Homocysteine levels
Title Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
Risk Allele A
P-val 3E-21
Odds Ratio .10 [0.079-0.123] unit decrease