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rs12470505

From SNPedia

Orientationplus
Stabilizedplus
Make rs12470505(G;G)
Make rs12470505(G;T)
Make rs12470505(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position219043647
is asnp
is mentioned by
dbSNPrs12470505
ebirs12470505
HLIrs12470505
Exacrs12470505
Varsomers12470505
Maprs12470505
PheGenIrs12470505
hapmaprs12470505
1000 genomesrs12470505
hgdprs12470505
ensemblrs12470505
gopubmedrs12470505
geneviewrs12470505
scholarrs12470505
googlers12470505
pharmgkbrs12470505
gwascentralrs12470505
openSNPrs12470505
23andMers12470505
23andMe allrs12470505
SNP Nexus

SNPshotrs12470505
SNPdbers12470505
MSV3drs12470505
GWAS Ctlgrs12470505
GMAF0.1703
Max Magnitude
? (G;G) (G;T) (T;T) 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 9E-12
Odds Ratio .04 [NR] unit increase