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rs10849432

From SNPedia

Orientationplus
Stabilizedplus
Make rs10849432(C;C)
Make rs10849432(C;T)
Make rs10849432(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position6276561
GeneLOC102723767
is asnp
is mentioned by
dbSNPrs10849432
ebirs10849432
HLIrs10849432
Exacrs10849432
Varsomers10849432
Maprs10849432
PheGenIrs10849432
hapmaprs10849432
1000 genomesrs10849432
hgdprs10849432
ensemblrs10849432
gopubmedrs10849432
geneviewrs10849432
scholarrs10849432
googlers10849432
pharmgkbrs10849432
gwascentralrs10849432
openSNPrs10849432
23andMers10849432
23andMe allrs10849432
SNP Nexus

SNPshotrs10849432
SNPdbers10849432
MSV3drs10849432
GWAS Ctlgrs10849432
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 T
P-val 6E-10
Odds Ratio 1.14 [1.09-1.18]