Disease: PERRAULT SYNDROME 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1561485663
rs1561485663
Entrez Id: 3295
Gene Symbol: HSD17B4
HSD17B4
CUI: C4551721
Disease:
PERRAULT SYNDROME 1 		G 0.700 CausalMutation CLINVAR