Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs222747
rs222747
0.010 GeneticVariation BEFREE Our results suggest novel genetic susceptibility to primary LPV associated with specific alleles in genes TRPV1 and NGF and propose the rs222747 "C" allele of TRPV1 as a common genetic predisposition for other pain syndromes. 30418350

2019

dbSNP: rs398123010
rs398123010
0.010 GeneticVariation BEFREE Remarkably, a substitution of single amino acid in the S4-S5 region of TRPA1 (N855S) has been recently associated with familial episodic pain syndrome. 24564660

2014

dbSNP: rs6746030
rs6746030
0.010 GeneticVariation BEFREE Genetic testing for ion channel-associated pain disorders revealed an amino acid R1150W substitution of the Nav1.7 sodium channel. 25116815

2014