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rs10774214

From SNPedia

Orientationplus
Stabilizedplus
Make rs10774214(C;C)
Make rs10774214(C;T)
Make rs10774214(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position4259186
is asnp
is mentioned by
dbSNPrs10774214
ebirs10774214
HLIrs10774214
Exacrs10774214
Varsomers10774214
Maprs10774214
PheGenIrs10774214
hapmaprs10774214
1000 genomesrs10774214
hgdprs10774214
ensemblrs10774214
gopubmedrs10774214
geneviewrs10774214
scholarrs10774214
googlers10774214
pharmgkbrs10774214
gwascentralrs10774214
openSNPrs10774214
23andMers10774214
23andMe allrs10774214
SNP Nexus

SNPshotrs10774214
SNPdbers10774214
MSV3drs10774214
GWAS Ctlgrs10774214
GMAF0.4394
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23263487OA-icon.png]
Trait Colorectal cancer
Title Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer.
Risk Allele T
P-val 5E-10
Odds Ratio 1.17 [1.11-1.23]
GWAS snp
PMID [PMID 24836286OA-icon.png]
Trait Colorectal cancer
Title Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
Risk Allele T
P-val 1E-10
Odds Ratio 1.14 [1.09-1.18]