Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064795638 0.851 0.080 3 52403251 stop gained G/A snv 7
rs768891111 0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27