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rs2972146

From SNPedia

Orientationminus
Stabilizedminus
Make rs2972146(A;A)
Make rs2972146(A;C)
Make rs2972146(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position226235982
is asnp
is mentioned by
dbSNPrs2972146
ebirs2972146
HLIrs2972146
Exacrs2972146
Varsomers2972146
Maprs2972146
PheGenIrs2972146
hapmaprs2972146
1000 genomesrs2972146
hgdprs2972146
ensemblrs2972146
gopubmedrs2972146
geneviewrs2972146
scholarrs2972146
googlers2972146
pharmgkbrs2972146
gwascentralrs2972146
openSNPrs2972146
23andMers2972146
23andMe allrs2972146
SNP Nexus

SNPshotrs2972146
SNPdbers2972146
MSV3drs2972146
GWAS Ctlgrs2972146
GMAF0.2259
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele C
P-val 2E-9
Odds Ratio 0.4600 None

[PMID 23659870OA-icon.png] Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study

GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele G
P-val 2E-17
Odds Ratio .03 [NR] unit increase