{{Rsnum
|rsid=12456021
|Gene=ALPK2
|Chromosome=18
|position=58546158
|Orientation=plus
|GMAF=0.2071
|Gene_s=ALPK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 34.5 | 62.8
| HCB | 6.6 | 45.3 | 48.2
| JPT | 8.0 | 38.9 | 53.1
| YRI | 0.0 | 6.9 | 93.1
| ASW | 0.0 | 14.0 | 86.0
| CHB | 6.6 | 45.3 | 48.2
| CHD | 11.0 | 45.0 | 44.0
| GIH | 5.0 | 31.7 | 63.4
| LWK | 0.9 | 2.7 | 96.4
| MEX | 10.3 | 53.4 | 36.2
| MKK | 0.0 | 4.5 | 95.5
| TSI | 2.9 | 35.3 | 61.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=A
  |Pval=4E-6
  |OR=1.10
  |ORtxt=[1.08-1.12]
  |OA=1
}}

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