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rs12603526

From SNPedia

Orientationplus
Stabilizedplus
Make rs12603526(C;C)
Make rs12603526(C;T)
Make rs12603526(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position897353
GeneNXN
is asnp
is mentioned by
dbSNPrs12603526
ebirs12603526
HLIrs12603526
Exacrs12603526
Varsomers12603526
Maprs12603526
PheGenIrs12603526
hapmaprs12603526
1000 genomesrs12603526
hgdprs12603526
ensemblrs12603526
gopubmedrs12603526
geneviewrs12603526
scholarrs12603526
googlers12603526
pharmgkbrs12603526
gwascentralrs12603526
openSNPrs12603526
23andMers12603526
23andMe allrs12603526
SNP Nexus

SNPshotrs12603526
SNPdbers12603526
MSV3drs12603526
GWAS Ctlgrs12603526
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 C
P-val 3E-8
Odds Ratio 1.10 [1.06-1.14]