Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518834
rs1057518834
DMD
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518905
rs1057518905
DPM3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518962
rs1057518962
DMD
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908188
rs121908188
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908457
rs121908457
MYOT ; LOC101928005
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554887097
rs1554887097
TWNK ; MRPL43
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1563083759
rs1563083759
TNPO3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1569518070
rs1569518070
COL6A1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs199564797
rs199564797
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201518227
rs201518227
TOR1AIP1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs543860009
rs543860009
TTN ; TTN-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs55960271
rs55960271
CLCN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs745886248
rs745886248
SELENON
A 0.700 GeneticVariation CLINVAR

dbSNP: rs757917335
rs757917335
DYSF
C 0.700 CausalMutation CLINVAR

dbSNP: rs80338800
rs80338800
CAPN3 ; LOC105370794
C 0.700 CausalMutation CLINVAR

dbSNP: rs878854378
rs878854378
TTN ; TTN-AS1
A 0.700 GeneticVariation CLINVAR