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rs13130787

From SNPedia

Orientationplus
Stabilizedplus
Make rs13130787(C;C)
Make rs13130787(C;T)
Make rs13130787(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position93965880
is asnp
is mentioned by
dbSNPrs13130787
ebirs13130787
HLIrs13130787
Exacrs13130787
Varsomers13130787
Maprs13130787
PheGenIrs13130787
hapmaprs13130787
1000 genomesrs13130787
hgdprs13130787
ensemblrs13130787
gopubmedrs13130787
geneviewrs13130787
scholarrs13130787
googlers13130787
pharmgkbrs13130787
gwascentralrs13130787
openSNPrs13130787
23andMers13130787
23andMe allrs13130787
SNP Nexus

SNPshotrs13130787
SNPdbers13130787
MSV3drs13130787
GWAS Ctlgrs13130787
GMAF0.326
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23266556OA-icon.png]
Trait Colorectal cancer
Title Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.
Risk Allele
P-val 3E-7
Odds Ratio 1.09 [1.06-1.13]