Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs6574978 0.925 0.080 14 88011069 synonymous variant C/T snv 0.75 0.72 2
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1042711 0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs584367 1.000 0.040 1 20115561 missense variant T/C snv 0.66 0.70 1
rs2243639 0.882 0.080 10 79941966 missense variant T/C;G snv 0.66 4
rs2571445 0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs13180 0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 7
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1136450 1.000 0.040 10 79611973 missense variant C/G snv 0.49 0.53 1
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs28381984 1.000 0.040 2 227270915 missense variant C/A;T snv 0.47 1
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs6609533 0.790 0.200 X 47585887 3 prime UTR variant A/G;T snv 0.46 7
rs1334576 1.000 0.040 6 7211585 missense variant G/A snv 0.45 0.40 2
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 11