Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs709399 0.882 0.080 14 103701208 3 prime UTR variant G/A snv 0.59 0.61 3
rs768891111 0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
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
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs4658973 0.882 0.080 1 117956431 intron variant T/G snv 0.34 3
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs145475805
TG
0.882 0.080 8 132887509 missense variant A/G snv 8.8E-05 3.3E-04 4
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10951937 0.882 0.080 7 47992027 intron variant A/C snv 0.43 3
rs180414 0.882 0.080 12 46775115 synonymous variant A/G snv 3.1E-03 3
rs776935407 0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 6
rs11214077 0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
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
rs1248131654 0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4