Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555421871
rs1555421871
6 0.882 0.120 15 42399617 frameshift variant G/- delins 0.700 0
dbSNP: rs1556962271
rs1556962271
DMD
2 0.925 0.120 X 31875197 frameshift variant -/AATG delins 0.700 0
dbSNP: rs1557058294
rs1557058294
DMD
1 1.000 0.120 X 32823294 splice donor variant C/T snv 0.700 0
dbSNP: rs1557396600
rs1557396600
DMD
2 0.925 0.120 X 32518006 splice donor variant A/C snv 0.700 0
dbSNP: rs1563083759
rs1563083759
6 0.925 0.120 7 128957260 frameshift variant G/- del 0.700 0
dbSNP: rs200916654
rs200916654
4 0.925 0.120 2 71551635 missense variant T/C snv 2.9E-05 0.700 0
dbSNP: rs202247792
rs202247792
5 0.925 0.120 6 129486605 missense variant T/C;G snv 8.0E-06 0.700 0
dbSNP: rs267607576
rs267607576
2 0.925 0.160 1 156136219 missense variant G/A;C snv 1.2E-05 0.700 0
dbSNP: rs267607634
rs267607634
2 0.925 0.120 1 156136045 missense variant G/A;C snv 0.700 0
dbSNP: rs267607644
rs267607644
1 1.000 0.120 1 156115022 missense variant T/C snv 0.700 0
dbSNP: rs387907298
rs387907298
2 0.925 0.200 17 50168562 stop gained C/T snv 5.7E-06 0.700 0
dbSNP: rs58932704
rs58932704
8 0.776 0.200 1 156136413 missense variant C/T snv 0.700 0
dbSNP: rs59332535
rs59332535
5 0.827 0.160 1 156134911 missense variant G/A snv 0.700 0
dbSNP: rs60458016
rs60458016
5 0.827 0.120 1 156136036 stop gained G/A;T snv 0.700 0
dbSNP: rs61672878
rs61672878
11 0.776 0.200 1 156136094 missense variant G/A;T snv 0.700 0
dbSNP: rs746438011
rs746438011
4 0.882 0.120 6 152430672 missense variant A/G;T snv 1.2E-05 0.700 0
dbSNP: rs755660222
rs755660222
1 1.000 0.120 14 77301228 frameshift variant C/- delins 1.2E-05 0.700 0
dbSNP: rs756015202
rs756015202
4 0.925 0.120 4 3493047 missense variant C/T snv 5.5E-06 0.700 0
dbSNP: rs757082154
rs757082154
9 1.000 0.120 2 178527491 stop gained G/A snv 1.2E-05 0.700 0
dbSNP: rs770905160
rs770905160
5 0.882 0.120 2 71656236 stop gained C/G;T snv 1.2E-05 0.700 0
dbSNP: rs778768583
rs778768583
10 0.851 0.120 15 42410958 missense variant G/C snv 8.0E-06 0.700 0
dbSNP: rs780302064
rs780302064
1 1.000 0.120 1 156137212 missense variant C/G;T snv 9.5E-06 0.700 0
dbSNP: rs797045898
rs797045898
1 1.000 0.120 14 77283874 splice acceptor variant CTAGG/TCA delins 0.700 0
dbSNP: rs80338800
rs80338800
21 0.827 0.120 15 42387803 frameshift variant A/- delins 0.700 0
dbSNP: rs886039785
rs886039785
DMD
7 0.925 0.120 X 31496876 stop gained C/T snv 0.700 0