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rs13177718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs13177718(C;T)
Make rs13177718(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position108777643
GeneFER
is asnp
is mentioned by
dbSNPrs13177718
ebirs13177718
HLIrs13177718
Exacrs13177718
Varsomers13177718
Maprs13177718
PheGenIrs13177718
hapmaprs13177718
1000 genomesrs13177718
hgdprs13177718
ensemblrs13177718
gopubmedrs13177718
geneviewrs13177718
scholarrs13177718
googlers13177718
pharmgkbrs13177718
gwascentralrs13177718
openSNPrs13177718
23andMers13177718
23andMe allrs13177718
SNP Nexus

SNPshotrs13177718
SNPdbers13177718
MSV3drs13177718
GWAS Ctlgrs13177718
GMAF0.03306
Max Magnitude0
? (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 3E-8
Odds Ratio .04 [NR] unit decrease