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rs17730929

From SNPedia

Orientationplus
Stabilizedplus
Make rs17730929(A;A)
Make rs17730929(A;C)
Make rs17730929(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position66491736
is asnp
is mentioned by
dbSNPrs17730929
ebirs17730929
HLIrs17730929
Exacrs17730929
Varsomers17730929
Maprs17730929
PheGenIrs17730929
hapmaprs17730929
1000 genomesrs17730929
hgdprs17730929
ensemblrs17730929
gopubmedrs17730929
geneviewrs17730929
scholarrs17730929
googlers17730929
pharmgkbrs17730929
gwascentralrs17730929
openSNPrs17730929
23andMers17730929
23andMe allrs17730929
SNP Nexus

SNPshotrs17730929
SNPdbers17730929
MSV3drs17730929
GWAS Ctlgrs17730929
GMAF0.04821
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23300701OA-icon.png]
Trait Colorectal cancer
Title Genome-wide search for gene-gene interactions in colorectal cancer.
Risk Allele
P-val 3E-6
Odds Ratio 1.47 [1.25-1.72]