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rs11196172

From SNPedia

Orientationplus
Stabilizedplus
Make rs11196172(A;A)
Make rs11196172(A;G)
Make rs11196172(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position112967084
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs11196172
ebirs11196172
HLIrs11196172
Exacrs11196172
Varsomers11196172
Maprs11196172
PheGenIrs11196172
hapmaprs11196172
1000 genomesrs11196172
hgdprs11196172
ensemblrs11196172
gopubmedrs11196172
geneviewrs11196172
scholarrs11196172
googlers11196172
pharmgkbrs11196172
gwascentralrs11196172
openSNPrs11196172
23andMers11196172
23andMe allrs11196172
SNP Nexus

SNPshotrs11196172
SNPdbers11196172
MSV3drs11196172
GWAS Ctlgrs11196172
Max Magnitude
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 A
P-val 1E-12
Odds Ratio 1.14 [1.10-1.18]


[PMID 27769063] Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.