{{Rsnum
|rsid=10999426
|Gene=PRF1
|Chromosome=10
|position=72360038
|Orientation=plus
|GMAF=0.1662
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.8 | 38.5 | 50.8
| HCB | 0.0 | 8.9 | 91.1
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 8.9 | 91.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20921521
|Title=Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis
}}{{PMID Auto
|PMID=16385451
|Title=A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
|OA=1
}}
{{PMID Auto
|PMID=23528102
|Title=Association between granzyme B and perforin I polymorphisms and allograft outcomes in Hispanic kidney transplant recipients
}}