Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
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
rs12343867 0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8
rs121913614
MPL
0.790 0.120 1 43349308 missense variant G/A snv 7
rs1057520016 0.851 0.080 9 5089726 missense variant C/A;T snv 5
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs562533120 0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3