Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs187558439
rs187558439
SCN9A ; SCN1A-AS1
0.010 GeneticVariation BEFREE We confirm through electrophysiological analysis that this R1488* variant in SCN9A results in complete loss-of-function of Na<sub>v</sub>1.7, which is consistent with reports on other variants in this gene in subjects with CIP. 30037327

2018