Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112374098
AR
0.925 0.200 X 67545417 stop gained C/A;T snv 2
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 2
rs1481151440
AR
1.000 0.160 X 67545467 stop gained C/A;T snv 1
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 3
rs1555996867
AR
1.000 0.160 X 67717603 missense variant C/G snv 1
rs768869912
AR
1.000 0.160 X 67717488 missense variant C/G snv 1.1E-05 1
rs1199988820
AR
1.000 0.160 X 67545363 stop gained C/G;T snv 7.3E-05 1
rs137852598
AR
1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 1
rs766161615
AR
1.000 0.160 X 67546589 stop gained C/G;T snv 5.8E-05 9.8E-06 1
rs773996740
AR
1.000 0.160 X 67546321 missense variant C/G;T snv 1.4E-05 1
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 3
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 3
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 2
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555997580
AR
0.925 0.200 X 67721873 stop gained C/T snv 2
rs201934623
AR
0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 2
rs886039558
AR
0.925 0.200 X 67717561 stop gained C/T snv 2
rs137852562
AR
0.925 0.160 X 67721837 missense variant C/T snv 1
rs137852575
AR
1.000 0.160 X 67545324 stop gained C/T snv 1
rs137852594
AR
1.000 0.160 X 67723745 synonymous variant C/T snv 1
rs1555969512
AR
1.000 0.160 X 67545360 stop gained C/T snv 1
rs1555969545
AR
1.000 0.160 X 67545414 stop gained C/T snv 1
rs1555990485
AR
1.000 0.160 X 67686087 missense variant C/T snv 1
rs1555995851
AR
1.000 0.160 X 67711620 missense variant C/T snv 1
rs1555995877
AR
1.000 0.160 X 67711687 missense variant C/T snv 1