Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356537
rs80356537
ATP1A3
T 0.700 CausalMutation CLINVAR Alternating hemiplegia of childhood. 8496742

1993
dbSNP: rs80356537
rs80356537
ATP1A3
T 0.700 CausalMutation CLINVAR Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. 2842249

1988