Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553264624
rs1553264624
LMNA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267607634
rs267607634
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs28936415
rs28936415
PMM2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs34997054
rs34997054
DYSF
A 0.700 GeneticVariation CLINVAR

dbSNP: rs549794342
rs549794342
NEB ; RIF1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs59332535
rs59332535
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs60458016
rs60458016
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs61672878
rs61672878
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs755660222
rs755660222
POMT2
A 0.700 CausalMutation CLINVAR

dbSNP: rs757082154
rs757082154
TTN ; TTN-AS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs769561386
rs769561386
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556962271
rs1556962271
DMD
AAATG 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265433
rs1553265433
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553265761
rs1553265761
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555421871
rs1555421871
CAPN3
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557396600
rs1557396600
DMD
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1563083759
rs1563083759
TNPO3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs200198778
rs200198778
POMT2
C 0.700 CausalMutation CLINVAR

dbSNP: rs200916654
rs200916654
DYSF
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607576
rs267607576
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607644
rs267607644
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs778768583
rs778768583
CAPN3
C 0.700 CausalMutation CLINVAR

dbSNP: rs80338800
rs80338800
CAPN3 ; LOC105370794
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518925
rs1057518925
COL6A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121908110
rs121908110
FKRP
G 0.700 CausalMutation CLINVAR