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rs4864201

From SNPedia

Orientationplus
Stabilizedplus
Make rs4864201(C;C)
Make rs4864201(C;T)
Make rs4864201(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position129810129
is asnp
is mentioned by
dbSNPrs4864201
ebirs4864201
HLIrs4864201
Exacrs4864201
Varsomers4864201
Maprs4864201
PheGenIrs4864201
hapmaprs4864201
1000 genomesrs4864201
hgdprs4864201
ensemblrs4864201
gopubmedrs4864201
geneviewrs4864201
scholarrs4864201
googlers4864201
pharmgkbrs4864201
gwascentralrs4864201
openSNPrs4864201
23andMers4864201
23andMe allrs4864201
SNP Nexus

SNPshotrs4864201
SNPdbers4864201
MSV3drs4864201
GWAS Ctlgrs4864201
GMAF0.4045
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22484627OA-icon.png]
Trait
Title A genome-wide association meta-analysis identifies new childhood obesity loci.
Risk Allele
P-val 2E-7
Odds Ratio 1.1240 None