rs869312877, CHD2

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Moderate intellectual disability
CUI: C0026351
Disease: Moderate intellectual disability
0.700 CausalMutation CLINVAR
EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
CUI: C3809278
Disease: EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
0.700 CausalMutation CLINVAR
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
0.700 CausalMutation CLINVAR