Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562159599
rs1562159599
WASF1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CCTGGC 0.700 CausalMutation CLINVAR De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. 29961568

2018