Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556165162
rs1556165162
HDAC8
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041936
rs886041936
HDAC8
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		A 0.700 CausalMutation CLINVAR