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rs10763546

From SNPedia

Orientationminus
Stabilizedplus
Make rs10763546(C;C)
Make rs10763546(C;G)
Make rs10763546(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position46059423
GeneTIMM23B
is asnp
is mentioned by
dbSNPrs10763546
ebirs10763546
HLIrs10763546
Exacrs10763546
Varsomers10763546
Maprs10763546
PheGenIrs10763546
hapmaprs10763546
1000 genomesrs10763546
hgdprs10763546
ensemblrs10763546
gopubmedrs10763546
geneviewrs10763546
scholarrs10763546
googlers10763546
pharmgkbrs10763546
gwascentralrs10763546
openSNPrs10763546
23andMers10763546
23andMe allrs10763546
SNP Nexus

SNPshotrs10763546
SNPdbers10763546
MSV3drs10763546
GWAS Ctlgrs10763546
GMAF0.4692
Max Magnitude
? (C;C) (C;G) (G;G) 28
Rs10763546
PubMed [PMID 18264097]
Affy Probeset SNP_A-8572122
Affy Orientation same
On GW 5.0 0
Alleles A/B C/G
Ancestral C
Population UK, Australia
Allele C
Case Freq.
Control Freq.
Odds Ratio Het 1.15
Odds Ratio Hom 1.99
Odds Ratio All
Disease Prostate cancer (PC)


rs10763546 is in linkage disequilibrium with a polymorphism that increases susceptibility to Prostate cancer 1.15 times for heterozygotes (CG) and 1.99 times for homozygotes (CC) [PMID 18264097]

rs10763546 is in linkage disequilibrium with a polymorphism that increases susceptibility to Prostate cancer 1.42 times for heterozygotes (CG) and 2.80 times for homozygotes (CC) [PMID 18264097]