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rs2142672

From SNPedia

Orientationminus
Stabilizedminus
Make rs2142672(C;C)
Make rs2142672(C;T)
Make rs2142672(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position16196963
is asnp
is mentioned by
dbSNPrs2142672
ebirs2142672
HLIrs2142672
Exacrs2142672
Varsomers2142672
Maprs2142672
PheGenIrs2142672
hapmaprs2142672
1000 genomesrs2142672
hgdprs2142672
ensemblrs2142672
gopubmedrs2142672
geneviewrs2142672
scholarrs2142672
googlers2142672
pharmgkbrs2142672
gwascentralrs2142672
openSNPrs2142672
23andMers2142672
23andMe allrs2142672
SNP Nexus

SNPshotrs2142672
SNPdbers2142672
MSV3drs2142672
GWAS Ctlgrs2142672
GMAF0.4844
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele C
P-val 2E-8
Odds Ratio 0.01 [0.007-0.015] unit increase