Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518938
rs1057518938
MYH11 ; NDE1
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs113422242
rs113422242
FBN1
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121918460
rs121918460
PTPN11
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		G 0.700 CausalMutation CLINVAR A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. 29555671

2018
dbSNP: rs1566911709
rs1566911709
FBN1
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		C 0.700 CausalMutation CLINVAR

dbSNP: rs397515804
rs397515804
FBN1
CUI: C0040961
Disease: Tricuspid Valve Insufficiency
Tricuspid Valve Insufficiency 		T 0.700 CausalMutation CLINVAR