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rs1014971

From SNPedia

Orientationminus
Stabilizedminus
Make rs1014971(A;A)
Make rs1014971(A;G)
Make rs1014971(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position38936618
is asnp
is mentioned by
dbSNPrs1014971
ebirs1014971
HLIrs1014971
Exacrs1014971
Varsomers1014971
Maprs1014971
PheGenIrs1014971
hapmaprs1014971
1000 genomesrs1014971
hgdprs1014971
ensemblrs1014971
gopubmedrs1014971
geneviewrs1014971
scholarrs1014971
googlers1014971
pharmgkbrs1014971
gwascentralrs1014971
openSNPrs1014971
23andMers1014971
23andMe allrs1014971
SNP Nexus

SNPshotrs1014971
SNPdbers1014971
MSV3drs1014971
GWAS Ctlgrs1014971
GMAF0.4858
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20972438OA-icon.png]
Trait
Title A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Risk Allele
P-val 8E-12
Odds Ratio 1.1800 [1.10-1.18]


[PMID 23284801OA-icon.png] Distinct SNP combinations confer susceptibility to urinary bladder cancer in smokers and non-smokers

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 T
P-val 1E-11
Odds Ratio 1.13 [1.09-1.17]


[PMID 27643540] Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors.