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rs3104964

From SNPedia

Orientationminus
Stabilizedminus
Make rs3104964(C;C)
Make rs3104964(C;T)
Make rs3104964(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position95583508
GeneGPRASP1
is asnp
is mentioned by
dbSNPrs3104964
ebirs3104964
HLIrs3104964
Exacrs3104964
Varsomers3104964
Maprs3104964
PheGenIrs3104964
hapmaprs3104964
1000 genomesrs3104964
hgdprs3104964
ensemblrs3104964
gopubmedrs3104964
geneviewrs3104964
scholarrs3104964
googlers3104964
pharmgkbrs3104964
gwascentralrs3104964
openSNPrs3104964
23andMers3104964
23andMe allrs3104964
SNP Nexus

SNPshotrs3104964
SNPdbers3104964
MSV3drs3104964
GWAS Ctlgrs3104964
GMAF0.438
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23350875OA-icon.png]
Trait Colorectal cancer
Title A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.
Risk Allele
P-val 4E-6
Odds Ratio 1.27 [1.144-1.398]