Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1032006770 0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs12628 0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs1064795638 0.851 0.080 3 52403251 stop gained G/A snv 7
rs1503185 0.807 0.120 11 48125070 missense variant G/A snv 0.18 0.19 8
rs1566734 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 10
rs10951937 0.882 0.080 7 47992027 intron variant A/C snv 0.43 3
rs2708896 0.882 0.080 7 47955186 upstream gene variant T/C;G snv 3
rs180414 0.882 0.080 12 46775115 synonymous variant A/G snv 3.1E-03 3
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs11077 0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
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
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs1800858
RET
0.851 0.160 10 43100520 synonymous variant A/C;G snv 0.73 4
rs776935407 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 6
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs63750447 0.716 0.200 3 37025749 missense variant T/A snv 2.7E-03 7.5E-04 17