Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2075685 0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs3749474 0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78