Rs10845271

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Orientationplus
Make rs10845271(C;C)
Make rs10845271(C;T)
Make rs10845271(T;T)
ReferenceGRCh37.p2 37.2/134
Chromosome12
Position11143801
GenePRH1, PRR4
is asnp
is mentioned by
dbSNPrs10845271
PheGenIrs10845271
nextbiors10845271
hapmaprs10845271
1000 genomesrs10845271
hgdprs10845271
ensemblrs10845271
gopubmedrs10845271
geneviewrs10845271
scholarrs10845271
googlers10845271
pharmgkbrs10845271
gwascentralrs10845271
openSNPrs10845271
23andMers10845271
23andMe allrs10845271
SNP Nexus

SNPshotrs10845271
SNPdbers10845271
MSV3drs10845271
GMAF0.4114
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs10845271
PubMed [PMID 16175505OA-icon.png]
Affy Probeset SNP_A-2027345
Affy Orientation same
On GW 5.0 1
Alleles A/B C/T
Ancestral C
Population Caucasian
Allele C
Case Freq.
Control Freq.
Odds Ratio Het 1.23
Odds Ratio Hom 1.58
Odds Ratio All
Disease Myocardial Infarction (MI)


rs10845271 is in linkage disequilibrium with a polymorphism that increases susceptibility to Myocardial Infarction 1.23 times for heterozygotes (CT) and 1.58 times for homozygotes (CC) [PMID 16175505OA-icon.png]