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rs2943650

From SNPedia

Orientationplus
Stabilizedplus
Make rs2943650(C;C)
Make rs2943650(C;T)
Make rs2943650(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position226241205
is asnp
is mentioned by
dbSNPrs2943650
ebirs2943650
HLIrs2943650
Exacrs2943650
Varsomers2943650
Maprs2943650
PheGenIrs2943650
hapmaprs2943650
1000 genomesrs2943650
hgdprs2943650
ensemblrs2943650
gopubmedrs2943650
geneviewrs2943650
scholarrs2943650
googlers2943650
pharmgkbrs2943650
gwascentralrs2943650
openSNPrs2943650
23andMers2943650
23andMe allrs2943650
SNP Nexus

SNPshotrs2943650
SNPdbers2943650
MSV3drs2943650
GWAS Ctlgrs2943650
GMAF0.3329
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21706003OA-icon.png]
Trait
Title Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
Risk Allele T
P-val 4E-11
Odds Ratio 0.0300 [NR] % decrease

[PMID 23659870OA-icon.png] Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study [PMID 22797928] Evidence of selection at insulin receptor substrate-1 gene loci.


[PMID 23708086] NUDT3 rs206936 is associated with body mass index in obese Japanese women.