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rs4980785

From SNPedia

Orientationplus
Stabilizedplus
Make rs4980785(C;C)
Make rs4980785(C;T)
Make rs4980785(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position69419726
is asnp
is mentioned by
dbSNPrs4980785
ebirs4980785
HLIrs4980785
Exacrs4980785
Varsomers4980785
Maprs4980785
PheGenIrs4980785
hapmaprs4980785
1000 genomesrs4980785
hgdprs4980785
ensemblrs4980785
gopubmedrs4980785
geneviewrs4980785
scholarrs4980785
googlers4980785
pharmgkbrs4980785
gwascentralrs4980785
openSNPrs4980785
23andMers4980785
23andMe allrs4980785
SNP Nexus

SNPshotrs4980785
SNPdbers4980785
MSV3drs4980785
GWAS Ctlgrs4980785
GMAF0.4688
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22010048OA-icon.png]
Trait
Title A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.
Risk Allele
P-val 0.000002
Odds Ratio None None