Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs1554700718 0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1569355102 0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1557043622 0.695 0.400 X 48909843 missense variant C/A snv 46
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs1557036768 0.708 0.320 X 53647390 missense variant C/T snv 44
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44