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rs4549702

From SNPedia

Orientationplus
Stabilizedplus
Make rs4549702(C;C)
Make rs4549702(C;G)
Make rs4549702(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position148203924
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs4549702
ebirs4549702
HLIrs4549702
Exacrs4549702
Varsomers4549702
Maprs4549702
PheGenIrs4549702
hapmaprs4549702
1000 genomesrs4549702
hgdprs4549702
ensemblrs4549702
gopubmedrs4549702
geneviewrs4549702
scholarrs4549702
googlers4549702
pharmgkbrs4549702
gwascentralrs4549702
openSNPrs4549702
23andMers4549702
23andMe allrs4549702
SNP Nexus

SNPshotrs4549702
SNPdbers4549702
MSV3drs4549702
GWAS Ctlgrs4549702
GMAF0.4197
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23192594OA-icon.png]
Trait Body mass index (interaction)
Title Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.
Risk Allele G
P-val 1E-6
Odds Ratio .01 [0.01-0.02] unit decrease