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rs494459

From SNPedia

Orientationminus
Stabilizedplus
Make rs494459(A;A)
Make rs494459(A;G)
Make rs494459(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position118703966
is asnp
is mentioned by
dbSNPrs494459
ebirs494459
HLIrs494459
Exacrs494459
Varsomers494459
Maprs494459
PheGenIrs494459
hapmaprs494459
1000 genomesrs494459
hgdprs494459
ensemblrs494459
gopubmedrs494459
geneviewrs494459
scholarrs494459
googlers494459
pharmgkbrs494459
gwascentralrs494459
openSNPrs494459
23andMers494459
23andMe allrs494459
SNP Nexus

SNPshotrs494459
SNPdbers494459
MSV3drs494459
GWAS Ctlgrs494459
GMAF0.405
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 2E-8
Odds Ratio .02 [NR] unit increase