Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs12493885 1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 1
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 1
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 2
rs1250259 1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 3
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs35489971 1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2838344 1.000 0.040 21 43669996 intron variant G/A snv 0.65 0.58 1
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs67180937 1.000 0.040 1 222650401 intron variant T/C;G snv 0.64 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2571445 0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 8
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3