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rs10094872

From SNPedia

Orientationplus
Stabilizedplus
Make rs10094872(A;A)
Make rs10094872(A;T)
Make rs10094872(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position127707639
GeneCASC11
is asnp
is mentioned by
dbSNPrs10094872
ebirs10094872
HLIrs10094872
Exacrs10094872
Varsomers10094872
Maprs10094872
PheGenIrs10094872
hapmaprs10094872
1000 genomesrs10094872
hgdprs10094872
ensemblrs10094872
gopubmedrs10094872
geneviewrs10094872
scholarrs10094872
googlers10094872
pharmgkbrs10094872
gwascentralrs10094872
openSNPrs10094872
23andMers10094872
23andMe allrs10094872
SNP Nexus

SNPshotrs10094872
SNPdbers10094872
MSV3drs10094872
GWAS Ctlgrs10094872
Max Magnitude
GWAS snp
PMID [PMID 24861552]
Trait Urinary bladder cancer
Title Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.
Risk Allele T
P-val 2E-7
Odds Ratio 1.26