{{Rsnum
|rsid=988213
|Gene=LOXHD1
|Chromosome=18
|position=46545004
|Orientation=plus
|GMAF=0.3714
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=LOXHD1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 39.3 | 37.5 | 23.2
| HCB | 21.9 | 50.4 | 27.7
| JPT | 15.9 | 38.9 | 45.1
| YRI | 98.0 | 2.0 | 0.0
| ASW | 66.7 | 29.8 | 3.5
| CHB | 21.9 | 50.4 | 27.7
| CHD | 21.1 | 43.1 | 35.8
| GIH | 63.4 | 32.7 | 4.0
| LWK | 92.7 | 7.3 | 0.0
| MEX | 36.2 | 39.7 | 24.1
| MKK | 85.3 | 14.7 | 0.0
| TSI | 46.1 | 37.3 | 16.7
| HapMapRevision=28
}}This SNP was associated with amyotrophic lateral sclerosis ([[ALS]]) based on a study of 1,152 patients.{{PMID|17671248}}

{{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}}
{{on chip | NatGeo2}}