Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482 0.685 0.393 4 1801837 missense variant C/T snp 23
rs119103263 0.821 0.143 1 11992659 missense variant C/T snp 19
rs121912854 0.846 0.107 3 48592915 stop gained G/A snp 1.2E-05 18
rs121912855 0.821 0.107 3 48575218 missense variant G/A snp 2.0E-05 17
rs74799832
RET
0.685 0.250 10 43121968 missense variant T/C snp 4.0E-06 16
rs1014959895 0.801 0.286 16 68329105 stop gained G/C,T snp 4.0E-06; 1.6E-05 15
rs199474657 0.744 0.321 MT 3243 non coding transcript exon variant snp 15
rs141322087 0.846 0.143 11 17404552 missense variant C/T snp 1.2E-05 3.2E-05 12
rs386834061 0.923 0.321 8 99868312 stop gained C/T snp 10
rs119473033 0.878 0.250 2 216478216 stop gained G/T snp 8.0E-05 1.6E-04 9
rs201431517 0.878 0.107 15 65021533 missense variant G/A snp 3.5E-04 4.8E-04 9
rs753242774 1.000 3 47848237 missense variant C/A,T snp 9
rs780261665 0.846 0.179 3 48590258 stop gained G/A snp 2.0E-05 9
rs1057518791 0.923 0.107 8 115604739 stop gained C/T snp 8
rs1057518907 0.878 0.179 20 58891811 stop gained C/T snp 8
rs113993993 0.923 0.179 7 66994210 splice donor variant A/C,G snp 4.0E-06; 3.9E-03 3.9E-03 8
rs748106387 0.923 0.071 2 216415427 stop gained C/A,T snp 2.8E-05 3.2E-05 8
rs1057518950
TPO
0.878 0.250 2 1484815 missense variant C/T snp 7
rs1057519436 0.878 0.179 3 47846550 missense variant G/A snp 7
rs1057518908 0.923 0.071 12 47984112 missense variant C/T snp 6
rs121434616 1.000 0.071 X 120544179 stop gained G/A snp 6
rs28933068 0.784 0.107 4 1805644 stop gained C/A,G,T snp 1.6E-05 6
rs1131691804 0.878 0.143 15 48463123 missense variant G/A snp 5
rs120074160 0.923 0.179 7 66994286 stop gained T/A snp 1.7E-04 9.9E-04 5
rs397517148 0.846 0.179 2 39023128 missense variant C/T snp 5