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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
GeneLOC107984591, MCF2L
is asnp
is mentioned by
dbSNPrs4907479
dbSNP (classic)rs4907479
ClinGenrs4907479
ebirs4907479
HLIrs4907479
Exacrs4907479
Gnomadrs4907479
Varsomers4907479
LitVarrs4907479
Maprs4907479
PheGenIrs4907479
Biobankrs4907479
1000 genomesrs4907479
hgdprs4907479
ensemblrs4907479
geneviewrs4907479
scholarrs4907479
googlers4907479
pharmgkbrs4907479
gwascentralrs4907479
openSNPrs4907479
23andMers4907479
SNPshotrs4907479
SNPdbers4907479
MSV3drs4907479
GWAS Ctlgrs4907479
Max Magnitude0
? (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]