Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
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
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
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
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34