{{Rsnum
|rsid=2603014
|Gene=LOC100996485
|Chromosome=5
|position=135307426
|Orientation=minus
|GMAF=0.3848
|Gene_s=LOC100996485
|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 | 44.2 | 46.0 | 9.7
| HCB | 73.7 | 24.1 | 2.2
| JPT | 80.5 | 18.6 | 0.9
| YRI | 6.8 | 44.2 | 49.0
| ASW | 15.8 | 40.4 | 43.9
| CHB | 73.7 | 24.1 | 2.2
| CHD | 78.0 | 21.1 | 0.9
| GIH | 56.4 | 33.7 | 9.9
| LWK | 16.4 | 47.3 | 36.4
| MEX | 34.5 | 48.3 | 17.2
| MKK | 10.9 | 43.6 | 45.5
| TSI | 38.2 | 42.2 | 19.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=22279524
|Title=Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases
|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}}