Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894780
rs104894780
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894782
rs104894782
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894784
rs104894784
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894785
rs104894785
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs122457137
rs122457137
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs1559193213
rs1559193213
SCN1A ; SCN1A-AS1 ; LOC102724058
TG 0.700 CausalMutation CLINVAR

dbSNP: rs201870761
rs201870761
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs267606317
rs267606317
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs56030372
rs56030372
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783518
rs587783518
DCX
C 0.700 CausalMutation CLINVAR

dbSNP: rs587783519
rs587783519
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783520
rs587783520
DCX
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783521
rs587783521
DCX
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783522
rs587783522
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783523
rs587783523
DCX
A 0.700 CausalMutation CLINVAR

dbSNP: rs587783524
rs587783524
DCX
G 0.700 CausalMutation CLINVAR

dbSNP: rs587783525
rs587783525
DCX
G 0.700 GeneticVariation CLINVAR

dbSNP: rs587783526
rs587783526
DCX
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783527
rs587783527
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783528
rs587783528
DCX
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783529
rs587783529
DCX
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783530
rs587783530
DCX
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783531
rs587783531
DCX
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587783532
rs587783532
DCX
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783533
rs587783533
DCX
A 0.700 CausalMutation CLINVAR