Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28937581
DYSF
0.827 0.160 2 71570300 missense variant G/T snv 1.2E-05 9
rs202218890
DYSF
0.827 0.160 2 71569884 missense variant C/T snv 4.0E-05 2.1E-05 5
rs121908955
DYSF
0.851 0.160 2 71682597 missense variant C/T snv 3.2E-05 2.1E-05 4
rs121908956
DYSF
0.851 0.160 2 71564074 missense variant C/A;G;T snv 4
rs121908958
DYSF
0.851 0.160 2 71570704 missense variant G/A snv 2.0E-05 6.3E-05 4
rs121908959
DYSF
0.851 0.120 2 71674242 stop gained C/T snv 1.2E-05 2.1E-05 4
rs140108514
DYSF
0.851 0.120 2 71568083 splice donor variant G/A snv 1.2E-04 4.5E-04 4
rs398123763
DYSF
0.851 0.120 2 71520905 splice donor variant G/A snv 2.1E-05 4
rs398123781
DYSF
0.851 0.120 2 71590212 stop gained TG/AA mnv 4
rs746873768
DYSF
0.851 0.120 2 71553092 stop gained C/T snv 1.2E-05 7.0E-06 4
rs758180890
DYSF
0.851 0.120 2 71526295 stop gained C/A;G;T snv 4.0E-06; 4.0E-06; 2.4E-05 4
rs121908957
DYSF
0.882 0.160 2 71481934 missense variant TG/AT mnv 3
rs121908963
DYSF
0.882 0.160 2 71517028 missense variant G/A;C;T snv 4.0E-06 3
rs727503909
DYSF
0.882 0.120 2 71568305 frameshift variant G/- delins 3
rs750028300
DYSF
0.882 0.120 2 71570277 missense variant T/C snv 4.0E-06 3
rs778171516
DMD
0.925 0.160 X 32595795 missense variant C/T snv 5.5E-06 2
rs121908962
DYSF
0.925 0.160 2 71551073 missense variant G/A snv 7.0E-06 2
rs1024524968
DYSF
1.000 2 71669673 missense variant G/A;C;T snv 1
rs121908953
DYSF
1.000 2 71553071 stop gained C/T snv 1