Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562159088
rs1562159088
A 0.700 CausalMutation CLINVAR De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. 29961568

2018

dbSNP: rs1562159562
rs1562159562
A 0.700 CausalMutation CLINVAR De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. 29961568

2018

dbSNP: rs1562159599
rs1562159599
CCTGGC 0.700 CausalMutation CLINVAR De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. 29961568

2018