Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730882262
rs730882262
LMNA
0.710 GeneticVariation BEFREE LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging. 25820511

2015
dbSNP: rs730882262
rs730882262
LMNA
G 0.710 CausalMutation CLINVAR

dbSNP: rs121912998
rs121912998
DSP ; LOC101928076
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1307997067
rs1307997067
TAX1BP3 ; P2RX5-TAX1BP3
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554108172
rs1554108172
DSP
T 0.700 GeneticVariation CLINVAR