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: rs886044913
rs886044913
TRIM32 ; ASTN2
1 9 116699102 frameshift variant -/TA delins 0.700 0
dbSNP: rs398123383
rs398123383
LAMA2
4 1.000 0.120 6 129460287 stop gained C/T snv 1.6E-05 7.0E-06 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
dbSNP: rs1208636573
rs1208636573
MSTO1 ; LOC105371452
15 0.807 0.120 1 155612098 stop gained C/G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs622288
rs622288
MSTO1 ; LOC105371452
15 0.807 0.120 1 155612848 missense variant C/T snv 3.6E-05 4.2E-05 0.700 0
dbSNP: rs201518227
rs201518227
TOR1AIP1
13 1.000 1 179917914 missense variant C/T snv 3.2E-05 5.6E-05 0.700 0
dbSNP: rs752298579
rs752298579
TANGO2
48 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs1555452876
rs1555452876
PKD1 ; MIR6511B1
5 1.000 16 2106222 inframe deletion CTC/- delins 0.700 0
dbSNP: rs137854521
rs137854521
ANO5
9 0.851 0.200 11 22221100 frameshift variant -/A delins 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: 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: rs1114167437
rs1114167437
DMD
1 X 31178681 frameshift variant T/- del 0.700 0
dbSNP: rs886044916
rs886044916
DMD
1 X 31209534 missense 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: rs1556880327
rs1556880327
DMD
2 X 31774182 frameshift variant -/T delins 0.700 0
dbSNP: rs1057516028
rs1057516028
DMD
1 X 32287680 stop gained G/A snv 0.700 0
dbSNP: rs1114167439
rs1114167439
DMD
1 X 32438240 splice donor variant C/- delins 0.700 0
dbSNP: rs1556980528
rs1556980528
DMD
1 X 32738791 intron variant T/C 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: 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: rs1555606976
rs1555606976
TCAP
1 17 39665448 frameshift variant GT/- delins 0.700 0
dbSNP: rs142239530
rs142239530
STIM1
24 0.790 0.320 11 4091328 missense variant C/G;T snv 4.4E-05 0.700 0
dbSNP: rs80338800
rs80338800
CAPN3 ; LOC105370794
21 0.827 0.120 15 42387803 frameshift variant A/- delins 0.700 0