Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs7309123 0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs5743313 0.851 0.200 4 186079213 intron variant C/T snv 0.19 4
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs1555580263 0.827 0.240 17 63837200 stop gained -/AGGTAGAACCTTATCTGCCATCTTC delins 6
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs1131692245 0.925 0.160 19 35844109 missense variant C/T snv 7
rs1057520529 0.851 0.320 X 49251440 missense variant C/T snv 5
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs1217371203 0.882 0.120 3 122106342 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs587782477
APC
0.882 0.120 5 112775679 missense variant A/T snv 4
rs868435969
VCP
0.925 0.280 9 35066710 missense variant G/A snv 3
rs4308977
CR2
0.925 0.160 1 207473553 missense variant T/A;C snv 4.0E-06; 0.27 2
rs17616
CR2
1.000 0.080 1 207473578 missense variant G/A snv 0.26 0.30 1