Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554643168
rs1554643168
PUF60
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554643168
rs1554643168
PUF60
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		G 0.700 GeneticVariation CLINVAR