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rs9360921

From SNPedia

Orientationplus
Stabilizedplus
Make rs9360921(G;G)
Make rs9360921(G;T)
Make rs9360921(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position75555926
is asnp
is mentioned by
dbSNPrs9360921
dbSNP (old)rs9360921
ClinGenrs9360921
ebirs9360921
HLIrs9360921
Exacrs9360921
Gnomadrs9360921
Varsomers9360921
Maprs9360921
PheGenIrs9360921
Biobankrs9360921
1000 genomesrs9360921
hgdprs9360921
ensemblrs9360921
gopubmedrs9360921
geneviewrs9360921
scholarrs9360921
googlers9360921
pharmgkbrs9360921
gwascentralrs9360921
openSNPrs9360921
23andMers9360921
23andMe allrs9360921
SNP Nexus

SNPshotrs9360921
SNPdbers9360921
MSV3drs9360921
GWAS Ctlgrs9360921
GMAF0.09366
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 3E-13
Odds Ratio 0.0400 [NR] meters decrease