Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59962885
DES
0.807 0.200 2 219420939 missense variant G/A;C;T snv 6.8E-05 11
rs1553603732
DES
1.000 0.160 2 219423784 frameshift variant CCCATCCAGACCTACTC/- delins 10
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs121913003
DES
0.882 0.200 2 219421532 missense variant C/T snv 6
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 6
rs57965306
DES
0.925 0.160 2 219421365 missense variant G/A;C snv 2.8E-05 6
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs62636495
DES
0.925 0.200 2 219418500 missense variant C/A;T snv 4
rs150974575
DES
1.000 0.160 2 219423817 stop gained C/T snv 1.2E-05 3
rs267607486
DES
1.000 0.160 2 219420346 missense variant G/A;C snv 3
rs58898021
DES
0.925 0.160 2 219421385 missense variant G/C snv 3
rs61726467
DES
0.882 0.160 2 219421553 stop gained G/A;T snv 3
rs267607483
DES
1.000 0.160 2 219420349 splice region variant A/G;T snv 2
rs267607485
DES
0.925 0.160 2 219425720 missense variant A/C snv 2
rs57639980
DES
1.000 0.160 2 219421350 missense variant T/C snv 2
rs60538473
DES
0.925 0.160 2 219418977 inframe deletion CGCGCGTCGACGTCGAGCGCG/- delins 2
rs60798368
DES
0.925 0.160 2 219418508 missense variant C/T snv 7.0E-06 2
rs61130669
DES
0.925 0.160 2 219421511 missense variant G/T snv 2
rs61368398
DES
1.000 0.160 2 219421380 missense variant G/A;C;T snv 3.2E-05 2
rs1057523274
DES
1.000 0.160 2 219418463 start lost A/G snv 1
rs1060503165
DES
1.000 0.160 2 219418856 stop gained C/T snv 1
rs121913000
DES
1.000 0.160 2 219421394 missense variant G/C snv 1
rs121913001
DES
1.000 0.160 2 219421494 missense variant A/G;T snv 1.2E-05 1
rs121913004
DES
1.000 0.160 2 219421482 missense variant A/C snv 1
rs121913005
DES
1.000 0.160 2 219425699 missense variant C/A;T snv 4.5E-06 1