Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2078371
rs2078371 		0.720 GeneticVariation BEFREE The SNP rs2078371 was found to be significantly associated with migraines especially in migraines without aura (MO) and in female patients. 30258394

2018
dbSNP: rs2078371
rs2078371 		C 0.720 GeneticVariation GWASCAT Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. 27322543

2016
dbSNP: rs2078371
rs2078371 		0.720 GeneticVariation BEFREE In addition, the C-allele of rs2078371 (near TSPAN-2) also reached genome-wide significance for association with migraine [OR = 1.14; CI = (1.09-1.20); P = 2.55 × 10(-8) ]. 23294458

2013