Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28939714 0.882 0.160 11 47582140 missense variant C/G;T snv 4.0E-06 3
rs746681765 0.882 0.080 5 110761543 missense variant C/A;T snv 2.8E-05 3
rs80356524 0.882 0.200 19 45553777 missense variant C/T snv 3
rs1020764190 0.925 0.120 18 12351330 missense variant G/A snv 2
rs104893753 0.925 0.080 3 193643005 stop gained C/T snv 2
rs1177373525 0.925 0.080 3 193666331 missense variant A/G snv 1.2E-05 2
rs1184021143 0.925 0.080 5 110761295 missense variant G/A snv 4.0E-06 2
rs1231502335 1.000 0.080 3 193643579 missense variant A/G snv 4.0E-06 1
rs779027563 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs374997012 0.851 0.280 10 100989114 missense variant C/T snv 8.0E-06 7.0E-06 9
rs759218713 0.882 0.080 1 29196235 missense variant T/C snv 8.0E-06 7.0E-06 3
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs587777175
TFG
0.925 0.080 3 100728759 missense variant C/T snv 4.0E-05 7.0E-06 2
rs730882240 1.000 0.080 16 574693 stop gained C/T snv 2.1E-05 3
rs762913101 0.882 0.080 1 29202004 missense variant C/T snv 7.2E-05 2.1E-05 3
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs397514477 0.925 0.080 19 29708415 missense variant G/A snv 8.0E-06 2.8E-05 5
rs104894270 0.882 0.160 11 47582436 missense variant C/T snv 1.6E-05 2.8E-05 3
rs34757931 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs145192716 0.882 0.080 1 29200574 missense variant G/A snv 6.4E-05 6.3E-05 3
rs756421370 0.807 0.120 1 29200513 splice donor variant -/A delins 1.4E-04 6.3E-05 8
rs139194636 0.882 0.240 1 119033203 missense variant T/C snv 6.4E-05 2.3E-04 6
rs151103940 0.882 0.160 3 193614929 missense variant A/G snv 4.0E-04 1.1E-03 3
rs201754030 0.925 0.200 12 57796461 stop gained C/T snv 1.5E-03 1.3E-03 5
rs284489 0.882 0.080 8 104945792 intron variant A/G snv 0.45 3