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rs516636

From SNPedia

Orientationplus
Stabilizedplus
Make rs516636(A;A)
Make rs516636(A;C)
Make rs516636(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position177886382
is asnp
is mentioned by
dbSNPrs516636
ebirs516636
HLIrs516636
Exacrs516636
Varsomers516636
Maprs516636
PheGenIrs516636
hapmaprs516636
1000 genomesrs516636
hgdprs516636
ensemblrs516636
gopubmedrs516636
geneviewrs516636
scholarrs516636
googlers516636
pharmgkbrs516636
gwascentralrs516636
openSNPrs516636
23andMers516636
23andMe allrs516636
SNP Nexus

SNPshotrs516636
SNPdbers516636
MSV3drs516636
GWAS Ctlgrs516636
GMAF0.1653
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22344221OA-icon.png]
Trait
Title Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
Risk Allele A
P-val 3E-9
Odds Ratio 0.0500 None