Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587784491
rs587784491
CUI: C1969029
Disease: Lissencephaly 3
Lissencephaly 3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs587784491
rs587784491
CUI: C1969029
Disease: Lissencephaly 3
Lissencephaly 3
T 0.700 CausalMutation CLINVAR