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rs12474201

From SNPedia

Orientationplus
Stabilizedplus
Make rs12474201(A;A)
Make rs12474201(A;G)
Make rs12474201(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46694146
is asnp
is mentioned by
dbSNPrs12474201
ebirs12474201
HLIrs12474201
Exacrs12474201
Varsomers12474201
Maprs12474201
PheGenIrs12474201
hapmaprs12474201
1000 genomesrs12474201
hgdprs12474201
ensemblrs12474201
gopubmedrs12474201
geneviewrs12474201
scholarrs12474201
googlers12474201
pharmgkbrs12474201
gwascentralrs12474201
openSNPrs12474201
23andMers12474201
23andMe allrs12474201
SNP Nexus

SNPshotrs12474201
SNPdbers12474201
MSV3drs12474201
GWAS Ctlgrs12474201
GMAF0.2585
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele A
P-val 3E-13
Odds Ratio 0.0300 [NR] meters increase