Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908425
rs121908425
CRMP1 ; EVC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1260978141
rs1260978141
DYNC2H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs137853027
rs137853027
DYNC2H1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1565311145
rs1565311145
DYNC2H1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565317399
rs1565317399
DYNC2H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1565329461
rs1565329461
DYNC2H1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1566883760
rs1566883760
KIAA0586
C 0.700 GeneticVariation CLINVAR

dbSNP: rs371011047
rs371011047
DYNC2H1
T 0.700 CausalMutation CLINVAR

dbSNP: rs376892534
rs376892534
DYNC2H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs752659088
rs752659088
KIAA0753
A 0.700 GeneticVariation CLINVAR

dbSNP: rs753317536
rs753317536
EVC
A 0.700 GeneticVariation CLINVAR

dbSNP: rs764926983
rs764926983
DYNC2H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs767846762
rs767846762
DYNC2H1
G 0.700 CausalMutation CLINVAR