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rs11046430

From SNPedia

Orientationplus
Stabilizedplus
Make rs11046430(C;C)
Make rs11046430(C;T)
Make rs11046430(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position22413495
is asnp
is mentioned by
dbSNPrs11046430
ebirs11046430
HLIrs11046430
Exacrs11046430
Varsomers11046430
Maprs11046430
PheGenIrs11046430
hapmaprs11046430
1000 genomesrs11046430
hgdprs11046430
ensemblrs11046430
gopubmedrs11046430
geneviewrs11046430
scholarrs11046430
googlers11046430
pharmgkbrs11046430
gwascentralrs11046430
openSNPrs11046430
23andMers11046430
23andMe allrs11046430
SNP Nexus

SNPshotrs11046430
SNPdbers11046430
MSV3drs11046430
GWAS Ctlgrs11046430
GMAF0.07071
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele T
P-val 4E-6
Odds Ratio .21 [0.13-0.29] unit decrease