Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs59885338
rs59885338
T 0.730 CausalMutation CLINVAR

dbSNP: rs142000963
rs142000963
T 0.700 GeneticVariation CLINVAR Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing. 25025039

2014

dbSNP: rs142000963
rs142000963
T 0.700 GeneticVariation CLINVAR Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C. 18478590

2008

dbSNP: rs57318642
rs57318642
T 0.700 CausalMutation CLINVAR

dbSNP: rs60864230
rs60864230
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356814
rs80356814
T 0.700 CausalMutation CLINVAR