Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs562533120 0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs318699 0.882 0.080 19 11390564 intron variant A/G snv 0.73 3
rs121913454 0.925 0.080 9 130874969 missense variant A/G snv 2
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs201478192 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs9376092 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs7046736 0.925 0.080 9 5015732 intron variant C/A snv 0.39 2
rs1057520016 0.851 0.080 9 5089726 missense variant C/A;T snv 5
rs770166362
MPL
1.000 0.040 1 43349298 missense variant C/G snv 4.0E-06 7.0E-06 1
rs750046020
MPL
0.827 0.080 1 43338646 missense variant C/G;T snv 8.0E-06; 8.0E-05 6
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs552479055 1.000 0.040 10 113726306 missense variant C/T snv 4.0E-06 1
rs78894077 1.000 0.040 12 111418869 missense variant C/T snv 2.7E-03 1.2E-03 1
rs587778514
MPL
0.925 0.080 1 43338564 frameshift variant CT/- del 5.2E-05 4.9E-05 2
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs121913614
MPL
0.790 0.120 1 43349308 missense variant G/A snv 7
rs10974947 0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs918140013 0.925 0.080 12 111447663 missense variant G/A snv 7.0E-06 2
rs1268279596 1.000 0.040 1 15495419 missense variant G/A snv 8.5E-06 1
rs746364606 1.000 0.040 3 184372642 missense variant G/A snv 1.2E-05 1.4E-05 1
rs28928907
MPL
0.882 0.160 1 43338634 missense variant G/A;C snv 8.0E-06; 3.8E-04 4
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 5