rs1057518162
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502047
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs111033590
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs111033592
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1411870484
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553488759
|
|
ACATTTTTGAATTCCTCAGT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1559027674
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs377543079
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs387906331
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs387906332
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs753900410
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs766212849
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs769971743
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs879253888
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553491169
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A novel Nav1.7 mutation producing carbamazepine-responsive erythromelalgia.
|
19557861 |
2009 |
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 |
rs1057518900
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Immunofluorescent and ultrastructural studies of polygonal microfilament networks in respreading non-muscle cells.
|
374104 |
1979 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |