Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1025993235 1.000 0.040 17 18865880 missense variant C/T snv 1
rs11231825 0.827 0.240 11 64592802 synonymous variant T/C snv 0.57 0.51 5
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs11554266 1.000 0.040 20 58903791 splice region variant C/G;T snv 4.0E-06; 2.3E-03 4
rs11602903 0.882 0.120 11 64590769 5 prime UTR variant A/T snv 0.51 3
rs1209613132 1.000 0.040 7 94404745 missense variant C/T snv 4.0E-06 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121907892 0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs1230053514 1.000 0.040 11 64598551 missense variant C/T snv 1
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs130154 1.000 0.040 22 48710770 intron variant C/T snv 0.69 1
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs141158222 1.000 0.040 20 53953466 missense variant C/T snv 1.2E-04 1.9E-04 1
rs141310123 0.925 0.120 18 79411390 missense variant C/A;T snv 2.1E-04; 4.8E-06 4
rs142226072 1.000 0.040 16 89637551 splice region variant C/T snv 2.2E-04 3.6E-04 1
rs143231463 1.000 0.040 6 7226577 missense variant A/G snv 1.8E-04 2.1E-04 3
rs143583842 1.000 0.040 16 20341262 missense variant G/A;T snv 7.4E-04; 1.2E-05 2
rs143709408 0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 5
rs147445322 0.882 0.120 11 2847803 missense variant G/A;T snv 7.2E-05; 5.5E-06 4
rs149454410 0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs149722479 0.925 0.200 11 64592788 missense variant G/A;C snv 4.8E-05; 9.6E-05 2
rs150801101 1.000 0.040 15 98957359 missense variant G/A snv 1.1E-04 3.6E-04 1
rs151305324 1.000 0.040 5 73123606 missense variant G/A snv 6.8E-05; 8.0E-06 9.1E-05 3