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rs6892884

From SNPedia

Orientationplus
Stabilizedplus
Make rs6892884(C;C)
Make rs6892884(C;T)
Make rs6892884(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position171588619
is asnp
is mentioned by
dbSNPrs6892884
ebirs6892884
HLIrs6892884
Exacrs6892884
Varsomers6892884
Maprs6892884
PheGenIrs6892884
hapmaprs6892884
1000 genomesrs6892884
hgdprs6892884
ensemblrs6892884
gopubmedrs6892884
geneviewrs6892884
scholarrs6892884
googlers6892884
pharmgkbrs6892884
gwascentralrs6892884
openSNPrs6892884
23andMers6892884
23andMe allrs6892884
SNP Nexus

SNPshotrs6892884
SNPdbers6892884
MSV3drs6892884
GWAS Ctlgrs6892884
GMAF0.2851
Max Magnitude
? (C;C) (C;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
P-val 4E-8
Odds Ratio NR NR