Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518925
rs1057518925
COL6A2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121908110
rs121908110
FKRP
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553264624
rs1553264624
LMNA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265369
rs1553265369
LMNA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265433
rs1553265433
LMNA
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553265436
rs1553265436
LMNA
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553265761
rs1553265761
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553521119
rs1553521119
DYSF
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553555585
rs1553555585
DYSF
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553846331
rs1553846331
DOK7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555421871
rs1555421871
CAPN3
C 0.700 CausalMutation CLINVAR

dbSNP: rs1556962271
rs1556962271
DMD
AAATG 0.700 GeneticVariation CLINVAR

dbSNP: rs1557058294
rs1557058294
DMD
T 0.700 GeneticVariation 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: rs202247792
rs202247792
LAMA2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs267607576
rs267607576
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607634
rs267607634
LMNA
A 0.700 CausalMutation CLINVAR

dbSNP: rs267607644
rs267607644
LMNA
C 0.700 GeneticVariation CLINVAR

dbSNP: rs28936415
rs28936415
PMM2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs34997054
rs34997054
DYSF
A 0.700 GeneticVariation CLINVAR

dbSNP: rs387907298
rs387907298
SGCA ; LOC105371818
T 0.700 CausalMutation CLINVAR

dbSNP: rs397517497
rs397517497
TTN
T 0.700 GeneticVariation CLINVAR