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rs7864648

From SNPedia

Orientationplus
Stabilizedplus
Make rs7864648(G;G)
Make rs7864648(G;T)
Make rs7864648(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position16368734
is asnp
is mentioned by
dbSNPrs7864648
ebirs7864648
HLIrs7864648
Exacrs7864648
Varsomers7864648
Maprs7864648
PheGenIrs7864648
hapmaprs7864648
1000 genomesrs7864648
hgdprs7864648
ensemblrs7864648
gopubmedrs7864648
geneviewrs7864648
scholarrs7864648
googlers7864648
pharmgkbrs7864648
gwascentralrs7864648
openSNPrs7864648
23andMers7864648
23andMe allrs7864648
SNP Nexus

SNPshotrs7864648
SNPdbers7864648
MSV3drs7864648
GWAS Ctlgrs7864648
GMAF0.3026
Max Magnitude
? (G;G) (G;T) (T;T) 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 T
P-val 2E-8
Odds Ratio 0.0200 [NR] meters increase