{{Rsnum
|rsid=13226650
|Gene=MLXIPL
|Chromosome=7
|position=73602675
|Orientation=plus
|GMAF=0.1763
|Gene_s=MLXIPL
|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 | 67.3 | 27.4 | 5.3
| HCB | 73.0 | 26.3 | 0.7
| JPT | 82.3 | 15.9 | 1.8
| YRI | 59.9 | 34.7 | 5.4
| ASW | 56.1 | 36.8 | 7.0
| CHB | 73.0 | 26.3 | 0.7
| CHD | 82.6 | 17.4 | 0.0
| GIH | 85.1 | 14.9 | 0.0
| LWK | 44.5 | 42.7 | 12.7
| MEX | 74.1 | 25.9 | 0.0
| MKK | 64.1 | 32.7 | 3.2
| TSI | 71.6 | 26.5 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22399527
|Trait=None
|Title=Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
|RiskAllele=A
|Pval=2E-11
|OR=0.1200
|ORtxt=None
|OA=1
}}

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