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rs7246657

From SNPedia

Orientationplus
Stabilizedplus
Make rs7246657(C;C)
Make rs7246657(C;T)
Make rs7246657(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position37256206
GeneAC012309.5
is asnp
is mentioned by
dbSNPrs7246657
ebirs7246657
HLIrs7246657
Exacrs7246657
Varsomers7246657
Maprs7246657
PheGenIrs7246657
hapmaprs7246657
1000 genomesrs7246657
hgdprs7246657
ensemblrs7246657
gopubmedrs7246657
geneviewrs7246657
scholarrs7246657
googlers7246657
pharmgkbrs7246657
gwascentralrs7246657
openSNPrs7246657
23andMers7246657
23andMe allrs7246657
SNP Nexus

SNPshotrs7246657
SNPdbers7246657
MSV3drs7246657
GWAS Ctlgrs7246657
GMAF0.3067
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 7E-6
Odds Ratio .16 [0.082-0.238] unit decrease