Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs118203478
rs118203478
TSC1
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1553511224
rs1553511224
TBR1
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs587776625
rs587776625
ADGRG1
T 0.700 CausalMutation CLINVAR

dbSNP: rs730882220
rs730882220
FAM20C
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869312693
rs869312693
DYNC1H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783562
rs587783562
DCX
0.010 GeneticVariation BEFREE We have studied the coding regions of the DCX gene in 11 Japanese patients with cortical dysplasia and have identified three different mutations (R186C in exon 3, R272X and R303X in exon 5) in four sporadic female cases. 10369164

1999