Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607485
DES
0.925 0.160 2 219425720 missense variant A/C snv 2
rs121913004
DES
1.000 0.160 2 219421482 missense variant A/C snv 1
rs1411703397
DES
1.000 0.160 2 219421359 missense variant A/C;T snv 4.0E-06 1
rs1057523274
DES
1.000 0.160 2 219418463 start lost A/G snv 1
rs1553603566
DES
1.000 0.160 2 219421467 missense variant A/G snv 1
rs267607482
DES
1.000 0.160 2 219421340 missense variant A/G snv 1
rs398122940
DES
1.000 0.160 2 219425661 splice acceptor variant A/G snv 1
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs267607483
DES
1.000 0.160 2 219420349 splice region variant A/G;T snv 2
rs121913001
DES
1.000 0.160 2 219421494 missense variant A/G;T snv 1.2E-05 1
rs886043000
DES
1.000 0.160 2 219418835 stop gained A/T snv 1
rs58687088
DES
1.000 0.160 2 219421410 inframe deletion ACA/- delins 1
rs730880289
DES
1.000 0.160 2 219420158 splice region variant AG/- delins 1
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs62636495
DES
0.925 0.200 2 219418500 missense variant C/A;T snv 4
rs121913005
DES
1.000 0.160 2 219425699 missense variant C/A;T snv 4.5E-06 1
rs60794845
DES
1.000 0.160 2 219418599 missense variant C/A;T snv 1
rs62635763
DES
1.000 0.160 2 219423787 missense variant C/A;T snv 1
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
rs150974575
DES
1.000 0.160 2 219423817 stop gained C/T snv 1.2E-05 3
rs60798368
DES
0.925 0.160 2 219418508 missense variant C/T snv 7.0E-06 2
rs1060503165
DES
1.000 0.160 2 219418856 stop gained C/T snv 1
rs1559352440
DES
1.000 0.160 2 219418976 stop gained C/T snv 1
rs267607488
DES
1.000 0.160 2 219425732 missense variant C/T snv 1