Gene: ATP1A2 ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs149144720
rs149144720
ATP1A2
A 0.700 GeneticVariation CLINVAR Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes. 24921013

2014
dbSNP: rs1553245857
rs1553245857
ATP1A2
A 0.700 CausalMutation CLINVAR Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes. 24921013

2014
dbSNP: rs1553245771
rs1553245771
ATP1A2
A 0.700 GeneticVariation CLINVAR Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation. 21352219

2011
dbSNP: rs149144720
rs149144720
ATP1A2
A 0.700 GeneticVariation CLINVAR De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine. 20837964

2010
dbSNP: rs149144720
rs149144720
ATP1A2
A 0.700 GeneticVariation CLINVAR Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. 19874388

2009
dbSNP: rs1553245857
rs1553245857
ATP1A2
A 0.700 CausalMutation CLINVAR Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. 19874388

2009
dbSNP: rs1165052640
rs1165052640
ATP1A2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918615
rs121918615
ATP1A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1226796744
rs1226796744
ATP1A2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1558008759
rs1558008759
ATP1A2
C 0.700 GeneticVariation CLINVAR