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rs6439167

From SNPedia

Orientationplus
Stabilizedplus
Make rs6439167(C;C)
Make rs6439167(C;T)
Make rs6439167(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position129331913
is asnp
is mentioned by
dbSNPrs6439167
ebirs6439167
HLIrs6439167
Exacrs6439167
Varsomers6439167
Maprs6439167
PheGenIrs6439167
hapmaprs6439167
1000 genomesrs6439167
hgdprs6439167
ensemblrs6439167
gopubmedrs6439167
geneviewrs6439167
scholarrs6439167
googlers6439167
pharmgkbrs6439167
gwascentralrs6439167
openSNPrs6439167
23andMers6439167
23andMe allrs6439167
SNP Nexus

SNPshotrs6439167
SNPdbers6439167
MSV3drs6439167
GWAS Ctlgrs6439167
GMAF0.1515
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 T
P-val 9E-15
Odds Ratio 0.03 [NR] unit decrease