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rs1027643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1027643(C;T)
Make rs1027643(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position92558085
is asnp
is mentioned by
dbSNPrs1027643
ebirs1027643
HLIrs1027643
Exacrs1027643
Varsomers1027643
Maprs1027643
PheGenIrs1027643
hapmaprs1027643
1000 genomesrs1027643
hgdprs1027643
ensemblrs1027643
gopubmedrs1027643
geneviewrs1027643
scholarrs1027643
googlers1027643
pharmgkbrs1027643
gwascentralrs1027643
openSNPrs1027643
23andMers1027643
23andMe allrs1027643
SNP Nexus

SNPshotrs1027643
SNPdbers1027643
MSV3drs1027643
GWAS Ctlgrs1027643
GMAF0.1832
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22544364OA-icon.png]
Trait
Title A genome-wide association study identifies susceptibility loci for Wilms tumor.
Risk Allele T
P-val 5E-10
Odds Ratio 1.4300 None