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rs8181166

From SNPedia

Orientationplus
Stabilizedplus
Make rs8181166(C;C)
Make rs8181166(C;G)
Make rs8181166(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position86501713
is asnp
is mentioned by
dbSNPrs8181166
ebirs8181166
HLIrs8181166
Exacrs8181166
Varsomers8181166
Maprs8181166
PheGenIrs8181166
hapmaprs8181166
1000 genomesrs8181166
hgdprs8181166
ensemblrs8181166
gopubmedrs8181166
geneviewrs8181166
scholarrs8181166
googlers8181166
pharmgkbrs8181166
gwascentralrs8181166
openSNPrs8181166
23andMers8181166
23andMe allrs8181166
SNP Nexus

SNPshotrs8181166
SNPdbers8181166
MSV3drs8181166
GWAS Ctlgrs8181166
GMAF0.3646
Max Magnitude
? (C;C) (C;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 C
P-val 3E-12
Odds Ratio .03 [NR] unit increase