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rs7763064

From SNPedia

Orientationplus
Stabilizedplus
Make rs7763064(A;A)
Make rs7763064(A;G)
Make rs7763064(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position142476152
is asnp
is mentioned by
dbSNPrs7763064
ebirs7763064
HLIrs7763064
Exacrs7763064
Varsomers7763064
Maprs7763064
PheGenIrs7763064
hapmaprs7763064
1000 genomesrs7763064
hgdprs7763064
ensemblrs7763064
gopubmedrs7763064
geneviewrs7763064
scholarrs7763064
googlers7763064
pharmgkbrs7763064
gwascentralrs7763064
openSNPrs7763064
23andMers7763064
23andMe allrs7763064
SNP Nexus

SNPshotrs7763064
SNPdbers7763064
MSV3drs7763064
GWAS Ctlgrs7763064
GMAF0.3921
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-33
Odds Ratio .05 [NR] unit decrease