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rs1257763

From SNPedia

Orientationplus
Stabilizedplus
Make rs1257763(A;A)
Make rs1257763(A;G)
Make rs1257763(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position94131663
is asnp
is mentioned by
dbSNPrs1257763
ebirs1257763
HLIrs1257763
Exacrs1257763
Varsomers1257763
Maprs1257763
PheGenIrs1257763
hapmaprs1257763
1000 genomesrs1257763
hgdprs1257763
ensemblrs1257763
gopubmedrs1257763
geneviewrs1257763
scholarrs1257763
googlers1257763
pharmgkbrs1257763
gwascentralrs1257763
openSNPrs1257763
23andMers1257763
23andMe allrs1257763
SNP Nexus

SNPshotrs1257763
SNPdbers1257763
MSV3drs1257763
GWAS Ctlgrs1257763
GMAF0.01423
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 A
P-val 1E-9
Odds Ratio .07 [NR] unit increase