{{Rsnum
|rsid=16966122
|Chromosome=19
|position=31667558
|Orientation=plus
|GMAF=0.1198
|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 | 72.6 | 23.9 | 3.5
| HCB | 83.9 | 16.1 | 0.0
| JPT | 83.2 | 15.0 | 1.8
| YRI | 66.7 | 29.3 | 4.1
| ASW | 78.9 | 17.5 | 3.5
| CHB | 83.9 | 16.1 | 0.0
| CHD | 80.7 | 18.3 | 0.9
| GIH | 75.2 | 21.8 | 3.0
| LWK | 77.3 | 20.0 | 2.7
| MEX | 87.9 | 12.1 | 0.0
| MKK | 87.2 | 12.8 | 0.0
| TSI | 81.4 | 15.7 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23496005
  |Trait=Narcolepsy with cataplexy
  |Title=Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.
  |RiskAllele=
  |Pval=2E-6
  |OR=1.60
  |ORtxt=[NR] unit decrease
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}