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rs10749971

From SNPedia

Orientationplus
Stabilizedplus
Make rs10749971(A;A)
Make rs10749971(A;G)
Make rs10749971(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position111318433
is asnp
is mentioned by
dbSNPrs10749971
ebirs10749971
HLIrs10749971
Exacrs10749971
Varsomers10749971
Maprs10749971
PheGenIrs10749971
hapmaprs10749971
1000 genomesrs10749971
hgdprs10749971
ensemblrs10749971
gopubmedrs10749971
geneviewrs10749971
scholarrs10749971
googlers10749971
pharmgkbrs10749971
gwascentralrs10749971
openSNPrs10749971
23andMers10749971
23andMe allrs10749971
SNP Nexus

SNPshotrs10749971
SNPdbers10749971
MSV3drs10749971
GWAS Ctlgrs10749971
GMAF0.2103
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22505654OA-icon.png] GWAS-identified colorectal cancer susceptibility loci associated with clinical outcomes


[PMID 18372901OA-icon.png] Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.


[PMID 19011631OA-icon.png] Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.