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rs7909670

From SNPedia

Orientationplus
Stabilizedplus
Make rs7909670(C;C)
Make rs7909670(C;T)
Make rs7909670(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position12876764
is asnp
is mentioned by
dbSNPrs7909670
ebirs7909670
HLIrs7909670
Exacrs7909670
Varsomers7909670
Maprs7909670
PheGenIrs7909670
hapmaprs7909670
1000 genomesrs7909670
hgdprs7909670
ensemblrs7909670
gopubmedrs7909670
geneviewrs7909670
scholarrs7909670
googlers7909670
pharmgkbrs7909670
gwascentralrs7909670
openSNPrs7909670
23andMers7909670
23andMe allrs7909670
SNP Nexus

SNPshotrs7909670
SNPdbers7909670
MSV3drs7909670
GWAS Ctlgrs7909670
GMAF0.4679
Max Magnitude
? (C;C) (C;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-9
Odds Ratio 0.0200 [NR] meters decrease