Source: ALL
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: rs1057516028
rs1057516028
DMD
1 X 32287680 stop gained G/A snv 0.700 0
dbSNP: rs116840795
rs116840795
CAV3 ; SSUH2
2 1.000 0.120 3 8745580 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs143570936
rs143570936
SGCA
5 0.925 0.200 17 50169246 missense variant G/A snv 1.1E-04 1.8E-04 0.700 0
dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
22 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 0.700 0
dbSNP: rs1131692158
rs1131692158
DYSF
5 1.000 0.120 2 71669207 missense variant G/A;C snv 0.700 0
dbSNP: rs116840778
rs116840778
CAV3 ; SSUH2
7 0.882 0.200 3 8733956 missense variant G/A;C snv 0.800 0
dbSNP: rs116840789
rs116840789
CAV3 ; SSUH2
6 0.925 0.080 3 8745547 missense variant G/A;T snv 0.700 0
dbSNP: rs375014127
rs375014127
ANO5
5 1.000 0.120 11 22262162 missense variant G/A;T snv 4.0E-06; 6.8E-05 0.700 0
dbSNP: rs914586984
rs914586984
SCN4A ; LOC105371858
9 1.000 0.120 17 63959275 missense variant G/C;T snv 0.700 0
dbSNP: rs1567825175
rs1567825175
GAA
1 17 80104590 stop gained G/T snv 0.700 0
dbSNP: rs1555606976
rs1555606976
TCAP
1 17 39665448 frameshift variant GT/- delins 0.700 0
dbSNP: rs1114167437
rs1114167437
DMD
1 X 31178681 frameshift variant T/- del 0.700 0
dbSNP: rs1556980528
rs1556980528
DMD
1 X 32738791 intron variant T/C snv 0.700 0
dbSNP: rs1559697515
rs1559697515
GMPPB
1 3 49723016 missense variant T/C snv 0.700 0
dbSNP: rs200916654
rs200916654
DYSF
4 0.925 0.120 2 71551635 missense variant T/C snv 2.9E-05 0.700 0
dbSNP: rs757917335
rs757917335
DYSF
6 1.000 0.120 2 71611481 missense variant T/C snv 2.0E-05 0.700 0
dbSNP: rs886044916
rs886044916
DMD
1 X 31209534 missense variant T/C snv 0.700 0
dbSNP: rs202247792
rs202247792
LAMA2
5 0.925 0.120 6 129486605 missense variant T/C;G snv 8.0E-06 0.700 0