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rs3782089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3782089(A;A)
Make rs3782089(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position65569348
GeneHMGB2
is asnp
is mentioned by
dbSNPrs3782089
ebirs3782089
HLIrs3782089
Exacrs3782089
Varsomers3782089
Maprs3782089
PheGenIrs3782089
hapmaprs3782089
1000 genomesrs3782089
hgdprs3782089
ensemblrs3782089
gopubmedrs3782089
geneviewrs3782089
scholarrs3782089
googlers3782089
pharmgkbrs3782089
gwascentralrs3782089
openSNPrs3782089
23andMers3782089
23andMe allrs3782089
SNP Nexus

SNPshotrs3782089
SNPdbers3782089
MSV3drs3782089
GWAS Ctlgrs3782089
GMAF0.05051
Max Magnitude0
? (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 T
P-val 4E-13
Odds Ratio 0.06 [NR] unit decrease