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rs1886449

From SNPedia

Orientationplus
Stabilizedplus
Make rs1886449(C;C)
Make rs1886449(C;T)
Make rs1886449(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position73357977
is asnp
is mentioned by
dbSNPrs1886449
ebirs1886449
HLIrs1886449
Exacrs1886449
Varsomers1886449
Maprs1886449
PheGenIrs1886449
hapmaprs1886449
1000 genomesrs1886449
hgdprs1886449
ensemblrs1886449
gopubmedrs1886449
geneviewrs1886449
scholarrs1886449
googlers1886449
pharmgkbrs1886449
gwascentralrs1886449
openSNPrs1886449
23andMers1886449
23andMe allrs1886449
SNP Nexus

SNPshotrs1886449
SNPdbers1886449
MSV3drs1886449
GWAS Ctlgrs1886449
GMAF0.2181
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20686608OA-icon.png]
Trait
Title Genome-wide association study of pancreatic cancer in Japanese population
Risk Allele A
P-val 0.000009
Odds Ratio 1.51 [1.26-1.80]