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rs8102137

From SNPedia

Orientationplus
Stabilizedplus
Make rs8102137(C;C)
Make rs8102137(C;T)
Make rs8102137(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position29805946
is asnp
is mentioned by
dbSNPrs8102137
dbSNP (classic)rs8102137
ClinGenrs8102137
ebirs8102137
HLIrs8102137
Exacrs8102137
Gnomadrs8102137
Varsomers8102137
LitVarrs8102137
Maprs8102137
PheGenIrs8102137
Biobankrs8102137
1000 genomesrs8102137
hgdprs8102137
ensemblrs8102137
geneviewrs8102137
scholarrs8102137
googlers8102137
pharmgkbrs8102137
gwascentralrs8102137
openSNPrs8102137
23andMers8102137
SNPshotrs8102137
SNPdbers8102137
MSV3drs8102137
GWAS Ctlgrs8102137
GMAF0.1736
Max Magnitude0
? (C;C) (C;T) (T;T) 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 C
P-val 2E-11
Odds Ratio 1.1300 [1.09-1.17]
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 C
P-val 1E-11
Odds Ratio 1.13 [1.09-1.17]


[PMID 27514407OA-icon.png] Transcription Factor KLF5 Binds a Cyclin E1 Polymorphic Intronic Enhancer to Confer Increased Bladder Cancer Risk.


[PMID 27738493OA-icon.png] Pathway analysis of bladder cancer genome-wide association study identifies novel pathways involved in bladder cancer development.


[PMID 29028944OA-icon.png] Identification and replication of the interplay of four genetic high risk variants for urinary bladder cancer.