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rs57046232

From SNPedia

Merged intors34033947
Orientationplus
Stabilizedplus
Make rs57046232(A;A)
Make rs57046232(A;T)
Make rs57046232(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position6399697
is asnp
is mentioned by
dbSNPrs57046232
dbSNP (classic)rs57046232
ClinGenrs57046232
ebirs57046232
HLIrs57046232
Exacrs57046232
Gnomadrs57046232
Varsomers57046232
LitVarrs57046232
Maprs57046232
PheGenIrs57046232
Biobankrs57046232
1000 genomesrs57046232
hgdprs57046232
ensemblrs57046232
geneviewrs57046232
scholarrs57046232
googlers57046232
pharmgkbrs57046232
gwascentralrs57046232
openSNPrs57046232
23andMers57046232
SNPshotrs57046232
SNPdbers57046232
MSV3drs57046232
GWAS Ctlgrs57046232
StatusMerged into rs34033947
Max Magnitude0
GWAS snp
PMID [PMID 24737748OA-icon.png]
Trait Colorectal cancer
Title Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Risk Allele T
P-val 3E-6
Odds Ratio 1.11 [NR]