{{Rsnum
|rsid=730566
|Gene=ATRIP
|Chromosome=3
|position=48445644
|Orientation=minus
|GMAF=0.3384
|Gene_s=ATRIP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 52.2 | 38.1 | 9.7
| HCB | 11.7 | 52.6 | 35.8
| JPT | 14.2 | 55.8 | 30.1
| YRI | 87.0 | 11.6 | 1.4
| ASW | 82.5 | 17.5 | 0.0
| CHB | 11.7 | 52.6 | 35.8
| CHD | 11.0 | 51.4 | 37.6
| GIH | 36.6 | 49.5 | 13.9
| LWK | 89.9 | 10.1 | 0.0
| MEX | 34.5 | 50.0 | 15.5
| MKK | 87.1 | 12.9 | 0.0
| TSI | 57.8 | 34.3 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22210626
|Trait=None
|Title=Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
|RiskAllele=
|Pval=0.000007
|OR=1.2700
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}