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rs4907479

From SNPedia

Orientationplus
Stabilizedplus
Make rs4907479(A;A)
Make rs4907479(A;G)
Make rs4907479(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113004794
GeneMCF2L
is asnp
is mentioned by
dbSNPrs4907479
ebirs4907479
HLIrs4907479
Exacrs4907479
Varsomers4907479
Maprs4907479
PheGenIrs4907479
hapmaprs4907479
1000 genomesrs4907479
hgdprs4907479
ensemblrs4907479
gopubmedrs4907479
geneviewrs4907479
scholarrs4907479
googlers4907479
pharmgkbrs4907479
gwascentralrs4907479
openSNPrs4907479
23andMers4907479
23andMe allrs4907479
SNP Nexus

SNPshotrs4907479
SNPdbers4907479
MSV3drs4907479
GWAS Ctlgrs4907479
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24163127OA-icon.png]
Trait Bladder cancer
Title Genome-wide association study identifies multiple loci associated with bladder cancer risk.
Risk Allele
P-val 3E-6
Odds Ratio 1.13 [1.07-1.18]