Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs4796793 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs4809957 0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10
rs50872 0.827 0.120 19 45359191 intron variant A/G;T snv 5
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs7211777 0.882 0.120 17 42382057 intron variant G/A snv 0.52 3
rs733618 0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs776223836 0.763 0.280 19 45364045 missense variant G/A snv 11
rs7867494 0.882 0.120 9 74529284 intron variant A/G snv 0.27 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
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs931127 0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs941759532 0.763 0.240 16 13932175 missense variant C/G snv 11
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37