Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518162
rs1057518162
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502047
rs1060502047
G 0.700 GeneticVariation CLINVAR

dbSNP: rs111033590
rs111033590
T 0.700 CausalMutation CLINVAR

dbSNP: rs111033592
rs111033592
T 0.700 CausalMutation CLINVAR

dbSNP: rs1411870484
rs1411870484
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553488759
rs1553488759
ACATTTTTGAATTCCTCAGT 0.700 CausalMutation CLINVAR

dbSNP: rs1559027674
rs1559027674
A 0.700 CausalMutation CLINVAR

dbSNP: rs377543079
rs377543079
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906331
rs387906331
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906332
rs387906332
T 0.700 CausalMutation CLINVAR

dbSNP: rs753900410
rs753900410
C 0.700 CausalMutation CLINVAR

dbSNP: rs766212849
rs766212849
A 0.700 CausalMutation CLINVAR

dbSNP: rs769971743
rs769971743
T 0.700 CausalMutation CLINVAR

dbSNP: rs879253888
rs879253888
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553491169
rs1553491169
T 0.700 GeneticVariation CLINVAR A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia. 19557861

2009

dbSNP: rs137852735
rs137852735
CA 0.700 CausalMutation CLINVAR Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates. 15060842

2004

dbSNP: rs1057518900
rs1057518900
A 0.700 CausalMutation CLINVAR Immunofluorescent and ultrastructural studies of polygonal microfilament networks in respreading non-muscle cells. 374104

1979

dbSNP: rs1295192882
rs1295192882
A 0.700 GeneticVariation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs187558439
rs187558439
A 0.700 CausalMutation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs746241591
rs746241591
A 0.700 GeneticVariation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs746241591
rs746241591
T 0.700 GeneticVariation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs755067851
rs755067851
T 0.700 GeneticVariation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs773824421
rs773824421
G 0.700 GeneticVariation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs779327684
rs779327684
CA 0.700 CausalMutation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132

2007

dbSNP: rs121908913
rs121908913
A 0.700 CausalMutation CLINVAR Nav1.7 mutations associated with paroxysmal extreme pain disorder, but not erythromelalgia, enhance Navbeta4 peptide-mediated resurgent sodium currents. 21115638

2011