Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15
rs63750949 0.827 0.080 2 47806213 missense variant C/A;T snv 6
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53