Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs138726443 0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs11584340 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs150597413 0.827 0.160 1 152305146 stop gained G/A;C;T snv 3.6E-05; 4.0E-06; 1.5E-03 5
rs2427837 0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20 5
rs3126085 0.851 0.280 1 152328341 intron variant G/A snv 0.29 5
rs941934 0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs121909626 0.882 0.120 1 152307225 stop gained G/C;T snv 2.0E-05 4
rs146466242 0.851 0.120 1 152302822 stop gained T/A;C snv 1.4E-03; 8.0E-06 4
rs6684514 0.925 0.120 1 156285665 missense variant G/A snv 0.27 0.24 4
rs7512552 1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs115746363 0.882 0.120 1 152312410 stop gained G/A;C snv 6.0E-04 3
rs149484917 0.882 0.120 1 152304939 stop gained G/C;T snv 4.7E-04; 4.0E-06 3
rs2251746 0.882 0.120 1 159302270 intron variant T/C snv 0.20 3
rs3001978 0.882 0.160 1 152153991 3 prime UTR variant T/C snv 0.50 3
rs7534334 0.882 0.160 1 153205376 downstream gene variant C/T snv 0.25 3
rs761212672 0.882 0.120 1 152304999 stop gained G/T snv 3.2E-05 3
rs11204971 0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs113136594 0.925 0.120 1 152313436 missense variant G/A;C;T snv 6.0E-04; 4.0E-06; 8.0E-06 2
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs12130219 0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2