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rs2890652

From SNPedia

Orientationplus
Stabilizedplus
Make rs2890652(C;C)
Make rs2890652(C;T)
Make rs2890652(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position142202362
is asnp
is mentioned by
dbSNPrs2890652
ebirs2890652
HLIrs2890652
Exacrs2890652
Varsomers2890652
Maprs2890652
PheGenIrs2890652
hapmaprs2890652
1000 genomesrs2890652
hgdprs2890652
ensemblrs2890652
gopubmedrs2890652
geneviewrs2890652
scholarrs2890652
googlers2890652
pharmgkbrs2890652
gwascentralrs2890652
openSNPrs2890652
23andMers2890652
23andMe allrs2890652
SNP Nexus

SNPshotrs2890652
SNPdbers2890652
MSV3drs2890652
GWAS Ctlgrs2890652
GMAF0.1625
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20935630OA-icon.png]
Trait
Title Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Risk Allele C
P-val 1E-10
Odds Ratio 0.09 [0.03-0.15] kg/m2 increase


[PMID 21953277] Association studies of novel obesity-related gene variants with quantitative metabolic phenotypes in a population-based sample of 6,039 Danish individuals.


[PMID 23471855OA-icon.png] The genetics of childhood obesity and interaction with dietary macronutrients.