Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs11655237 0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 17