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rs4754373

From SNPedia

Orientationplus
Stabilizedplus
Make rs4754373(C;C)
Make rs4754373(C;T)
Make rs4754373(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position109022119
is asnp
is mentioned by
dbSNPrs4754373
ebirs4754373
HLIrs4754373
Exacrs4754373
Varsomers4754373
Maprs4754373
PheGenIrs4754373
hapmaprs4754373
1000 genomesrs4754373
hgdprs4754373
ensemblrs4754373
gopubmedrs4754373
geneviewrs4754373
scholarrs4754373
googlers4754373
pharmgkbrs4754373
gwascentralrs4754373
openSNPrs4754373
23andMers4754373
23andMe allrs4754373
SNP Nexus

SNPshotrs4754373
SNPdbers4754373
MSV3drs4754373
GWAS Ctlgrs4754373
GMAF0.2314
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19461586OA-icon.png] Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study