Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12425451
rs12425451
0.700 GeneticVariation GWASDB Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study. 23496005

2013

dbSNP: rs17212223
rs17212223
T 0.700 GeneticVariation GWASCAT Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. 24204295

2013

dbSNP: rs2859998
rs2859998
0.700 GeneticVariation GWASDB Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study. 23496005

2013

dbSNP: rs7744020
rs7744020
A 0.700 GeneticVariation GWASCAT Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. 24204295

2013

dbSNP: rs9274477
rs9274477
G 0.700 GeneticVariation GWASCAT Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. 24204295

2013

dbSNP: rs1154155
rs1154155
0.010 GeneticVariation BEFREE Single-nucleotide polymorphism (SNP) rs1154155 located in the T-cell receptor alpha (TCRA) locus has been recently identified as a novel genetic marker of susceptibility for narcolepsy with cataplexy. 19927159

2010

dbSNP: rs5770917
rs5770917
0.010 GeneticVariation BEFREE SNP rs5770917 located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype were previously identified as susceptibility loci for narcolepsy with cataplexy. 19404393

2009