Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934897
MVK
0.790 0.400 12 109596515 missense variant G/A snv 1.6E-03 1.5E-03 10
rs104895304
MVK
0.827 0.280 12 109591275 missense variant T/C snv 1.5E-04 1.7E-04 5
rs7134594
MMAB
1.000 0.200 12 109562388 intron variant C/G;T snv 4
rs104895319
MVK
0.851 0.240 12 109595070 missense variant G/A snv 2.0E-05 7.0E-06 4
rs104895321
MVK
0.882 0.240 12 109591301 missense variant C/G;T snv 1.4E-04 4
rs104895382
MVK
0.851 0.240 12 109579921 missense variant T/C snv 3.2E-05 7.0E-05 4
rs104895297
MVK
0.882 0.360 12 109581427 missense variant C/T snv 3
rs104895308
MVK
0.882 0.200 12 109595118 missense variant G/A snv 3
rs778608015
ANXA5
0.925 0.200 4 121669702 missense variant G/A;C snv 8.0E-06 2
rs138258349
DNAH8
0.925 0.200 6 38737215 missense variant T/C snv 6.4E-05 3.7E-04 2
rs1450500
GRID2
1.000 0.200 4 92558124 intron variant A/G snv 0.69 2
rs753716740
IL4I1 ; NUP62
0.925 0.200 19 49909002 missense variant G/A snv 4.0E-06 2
rs144069312
MMAB ; MVK
0.925 0.200 12 109574893 missense variant A/C snv 4.1E-06; 4.1E-06 7.0E-06 2
rs11614976
MVK
0.925 0.200 12 109595145 missense variant G/A snv 2
rs121917789
MVK
0.925 0.200 12 109595044 missense variant A/C;G snv 4.0E-06 2
rs148576029
MVK
0.925 0.200 12 109590850 missense variant A/T snv 4.0E-06 2
rs202172198
MVK
0.925 0.200 12 109586086 missense variant G/A;C;T snv 1.6E-05; 4.0E-06; 4.0E-06 2
rs372446928
NUP62 ; IL4I1
0.925 0.200 19 49909008 missense variant G/A snv 1.6E-05 2
rs185313167
SQSTM1
0.925 0.200 5 179833083 missense variant C/T snv 8.0E-06 2
rs104895127
MEFV
1.000 0.200 16 3254342 missense variant G/A;C;T snv 8.0E-06; 4.0E-06 1
rs104895366
MVK
1.000 0.200 12 109590802 missense variant A/T snv 1.6E-05 7.0E-06 1
rs1304512133
NLRC4
1.000 0.200 2 32251138 missense variant C/G;T snv 4.0E-06 1
rs146442638
NLRP3
1.000 0.200 1 247424238 missense variant C/A;T snv 8.0E-06; 1.7E-04 1