{{Rsnum
|rsid=10845271
|Gene=PRH1
|Chromosome=12
|position=11143801
|Orientation=plus
|GMAF=0.4114
|Gene_s=PRH1,PRR4
|Assembly=GRCh37.p2
|GenomeBuild=37.2
|dbSNPBuild=134
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 45.0 | 43.2 | 11.7
| HCB | 5.1 | 39.7 | 55.1
| JPT | 8.0 | 31.9 | 60.2
| YRI | 88.2 | 11.8 | 0.0
| ASW | 75.9 | 24.1 | 0.0
| CHB | 5.1 | 39.7 | 55.1
| CHD | 10.1 | 35.8 | 54.1
| GIH | 14.0 | 41.0 | 45.0
| LWK | 89.9 | 9.2 | 0.9
| MEX | 15.8 | 59.6 | 24.6
| MKK | 74.4 | 25.0 | 0.6
| TSI | 28.0 | 51.0 | 21.0
| HapMapRevision=28
}}

{{Report GE
|PubMed=16175505
|Source=GADB
|AffyProbeset=SNP_A-2027345
|AffyOrientation=same
|AlleleA=C
|AlleleB=T
|onGW5=1
|rsid=10845271
|ancestral=C
|RiskPopulation=Caucasian
|RiskAllele=C
|CaseFreq=
|ControlFreq=
|OddsRatioHet=1.23
|OddsRatioHom=1.58
|OddsRatioAll=
|Disease=Myocardial Infarction
|DiseaseSymbol=MI
|OA=1
}}

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|16175505|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}