Have questions? Visit https://www.reddit.com/r/SNPedia

rs7027110

From SNPedia

Orientationplus
Stabilizedplus
Make rs7027110(A;A)
Make rs7027110(A;G)
Make rs7027110(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position106836765
is asnp
is mentioned by
dbSNPrs7027110
dbSNP (classic)rs7027110
ClinGenrs7027110
ebirs7027110
HLIrs7027110
Exacrs7027110
Gnomadrs7027110
Varsomers7027110
LitVarrs7027110
Maprs7027110
PheGenIrs7027110
Biobankrs7027110
1000 genomesrs7027110
hgdprs7027110
ensemblrs7027110
geneviewrs7027110
scholarrs7027110
googlers7027110
pharmgkbrs7027110
gwascentralrs7027110
openSNPrs7027110
23andMers7027110
SNPshotrs7027110
SNPdbers7027110
MSV3drs7027110
GWAS Ctlgrs7027110
GMAF0.1841
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 A
P-val 2E-13
Odds Ratio .03 [NR] unit increase