Gene: SCN1A-AS1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755067851
rs755067851
SCN9A ; SCN1A-AS1
T 0.700 GeneticVariation CLINVAR Two novel SCN9A mutations causing insensitivity to pain. 19304393

2009
dbSNP: rs766212849
rs766212849
SCN9A ; SCN1A-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs769971743
rs769971743
SCN9A ; SCN1A-AS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs773824421
rs773824421
SCN9A ; SCN1A-AS1
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: rs773824421
rs773824421
SCN9A ; SCN1A-AS1
G 0.700 GeneticVariation CLINVAR Two novel SCN9A mutations causing insensitivity to pain. 19304393

2009
dbSNP: rs779327684
rs779327684
SCN9A ; SCN1A-AS1
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