Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886028 1.000 0.080 12 25227308 missense variant C/T snv 1
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs1057519855 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs11214077 0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1188536960 0.882 0.120 15 45043305 missense variant A/G snv 5
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 18
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 19
rs121913306
RET
0.851 0.120 10 43120119 missense variant AGC/TTT mnv 4
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 4
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs143795581
RET
0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06 2
rs145633958
RET
1.000 0.080 10 43100551 missense variant C/A;T snv 2.7E-03; 4.0E-06 1
rs146646971
RET
0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 5
rs146838520
RET
0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 4
rs148935214
RET
0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 3
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs1800863
RET
0.851 0.160 10 43120185 synonymous variant C/A;G snv 1.6E-05; 0.21 4
rs183334241 0.925 0.080 18 75288186 missense variant G/A;C snv 1.6E-04 2
rs2075912
RET
0.925 0.160 10 43126769 3 prime UTR variant T/C snv 0.79 0.84 2
rs2565200
RET
0.925 0.160 10 43127485 3 prime UTR variant T/A;C snv 2
rs3026785
RET
1.000 0.080 10 43130238 3 prime UTR variant T/C snv 4.3E-02 1
rs33927012 1.000 0.080 1 17027802 missense variant A/G snv 1.2E-02 9.3E-03 1