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rs11903757

From SNPedia

Orientationplus
Stabilizedplus
Make rs11903757(C;C)
Make rs11903757(C;T)
Make rs11903757(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position191722478
is asnp
is mentioned by
dbSNPrs11903757
ebirs11903757
HLIrs11903757
Exacrs11903757
Varsomers11903757
Maprs11903757
PheGenIrs11903757
hapmaprs11903757
1000 genomesrs11903757
hgdprs11903757
ensemblrs11903757
gopubmedrs11903757
geneviewrs11903757
scholarrs11903757
googlers11903757
pharmgkbrs11903757
gwascentralrs11903757
openSNPrs11903757
23andMers11903757
23andMe allrs11903757
SNP Nexus

SNPshotrs11903757
SNPdbers11903757
MSV3drs11903757
GWAS Ctlgrs11903757
GMAF0.1249
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23266556OA-icon.png] Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-Analysis


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