Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs3798577 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16