Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs137854539 0.716 0.520 20 58903703 missense variant C/T snv 28
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 12
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 11
rs104893689 0.790 0.200 3 122261589 missense variant G/A;C snv 10
rs193922442 0.827 0.120 3 122261589 frameshift variant G/- del 5
rs767363250 0.827 0.280 3 122283992 missense variant C/T snv 4.0E-06 7.0E-06 5
rs61734277 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs201858689 0.882 0.120 3 122284257 missense variant G/T snv 2.8E-05 3
rs6254
PTH
0.925 0.080 11 13492716 intron variant C/A;T snv 4.0E-06; 0.28 2