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rs1468758

From SNPedia

Orientationplus
Stabilizedplus
Make rs1468758(C;C)
Make rs1468758(C;T)
Make rs1468758(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position111044802
is asnp
is mentioned by
dbSNPrs1468758
ebirs1468758
HLIrs1468758
Exacrs1468758
Varsomers1468758
Maprs1468758
PheGenIrs1468758
hapmaprs1468758
1000 genomesrs1468758
hgdprs1468758
ensemblrs1468758
gopubmedrs1468758
geneviewrs1468758
scholarrs1468758
googlers1468758
pharmgkbrs1468758
gwascentralrs1468758
openSNPrs1468758
23andMers1468758
23andMe allrs1468758
SNP Nexus

SNPshotrs1468758
SNPdbers1468758
MSV3drs1468758
GWAS Ctlgrs1468758
GMAF0.3269
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 1E-9
Odds Ratio .03 [NR] unit decrease