Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1114167628 0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 5
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1172398253 0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
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
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs3741219 0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs376066276 0.925 0.080 11 4390219 missense variant C/A;T snv 4.0E-06; 8.0E-06 4
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs80358829 0.827 0.120 13 32340327 missense variant C/T snv 6
rs868257011 0.925 0.080 10 87961042 frameshift variant TACTT/- del 4
rs1056123575 0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1213469537 0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9