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: rs137854521
rs137854521
ANO5
9 0.851 0.200 11 22221100 frameshift variant -/A delins 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: rs776474397
rs776474397
ANO5
1 11 22227300 splice acceptor variant A/G snv 0.700 0
dbSNP: rs886044915
rs886044915
ANO5
1 11 22236272 missense variant A/C snv 0.700 0
dbSNP: rs201892814
rs201892814
CAPN3
8 1.000 0.040 15 42403721 intron variant C/G snv 3.1E-03; 2.4E-05 3.1E-03 0.700 0
dbSNP: rs768090444
rs768090444
CAPN3
3 1.000 0.120 15 42410645 stop gained C/G;T snv 4.0E-06 2.1E-05 0.700 0
dbSNP: rs80338800
rs80338800
CAPN3 ; LOC105370794
21 0.827 0.120 15 42387803 frameshift variant A/- delins 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: rs116840786
rs116840786
CAV3 ; SSUH2
1 3 8733962 missense variant C/A;T 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: 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: rs1057516028
rs1057516028
DMD
1 X 32287680 stop gained G/A snv 0.700 0
dbSNP: rs1114167437
rs1114167437
DMD
1 X 31178681 frameshift variant T/- del 0.700 0
dbSNP: rs1114167439
rs1114167439
DMD
1 X 32438240 splice donor variant C/- delins 0.700 0
dbSNP: rs1556880327
rs1556880327
DMD
2 X 31774182 frameshift variant -/T delins 0.700 0
dbSNP: rs1556980528
rs1556980528
DMD
1 X 32738791 intron variant T/C snv 0.700 0
dbSNP: rs886039785
rs886039785
DMD
7 0.925 0.120 X 31496876 stop gained C/T snv 0.700 0
dbSNP: rs886042604
rs886042604
DMD
3 1.000 0.120 X 33020138 splice donor variant C/G;T snv 0.700 0
dbSNP: rs886044916
rs886044916
DMD
1 X 31209534 missense variant T/C snv 0.700 0
dbSNP: rs1553846331
rs1553846331
DOK7
4 0.925 0.120 4 3473504 missense variant C/T snv 0.700 0
dbSNP: rs756015202
rs756015202
DOK7
4 0.925 0.120 4 3493047 missense variant C/T snv 5.5E-06 0.700 0
dbSNP: rs1131692158
rs1131692158
DYSF
5 1.000 0.120 2 71669207 missense variant G/A;C snv 0.700 0
dbSNP: rs1553521119
rs1553521119
DYSF
5 0.925 0.120 2 71513892 frameshift variant C/- del 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