Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
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
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs121912473 0.925 0.080 9 5070026 missense variant AA/TT mnv 3
rs12339666 0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs17849241 0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs2201862 0.925 0.080 3 168930251 downstream gene variant T/C snv 0.63 3
rs4495487 0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs562533120 0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3
rs1200469268 0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2