{{Rsnum
|rsid=10108954
|Gene=MFHAS1
|Chromosome=8
|position=8864868
|Orientation=plus
|GMAF=0.1143
|Gene_s=MFHAS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 92.0 | 8.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 29.3 | 50.3 | 20.4
| ASW | 36.8 | 52.6 | 10.5
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 79.2 | 15.8 | 5.0
| LWK | 37.3 | 49.1 | 13.6
| MEX | 84.5 | 15.5 | 0.0
| MKK | 51.6 | 39.4 | 9.0
| TSI | 92.2 | 7.8 | 0.0
| 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=1.7359
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}