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rs7332115

From SNPedia

Orientationplus
Stabilizedplus
Make rs7332115(G;G)
Make rs7332115(G;T)
Make rs7332115(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32573411
is asnp
is mentioned by
dbSNPrs7332115
dbSNP (classic)rs7332115
ClinGenrs7332115
ebirs7332115
HLIrs7332115
Exacrs7332115
Gnomadrs7332115
Varsomers7332115
LitVarrs7332115
Maprs7332115
PheGenIrs7332115
Biobankrs7332115
1000 genomesrs7332115
hgdprs7332115
ensemblrs7332115
geneviewrs7332115
scholarrs7332115
googlers7332115
pharmgkbrs7332115
gwascentralrs7332115
openSNPrs7332115
23andMers7332115
SNPshotrs7332115
SNPdbers7332115
MSV3drs7332115
GWAS Ctlgrs7332115
GMAF0.2998
Max Magnitude0
? (G;G) (G;T) (T;T) 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 T
P-val 6E-10
Odds Ratio .02 [NR] unit decrease