Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 3
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs377767391
RET
0.827 0.160 10 43113627 missense variant T/A;C;G snv 2
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs75030001
RET
0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 2
rs77316810
RET
0.776 0.200 10 43113654 missense variant T/A;C;G snv 2
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 2
rs80069458
RET
0.882 0.120 10 43113629 missense variant C/G;T snv 2
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs377767397
RET
0.790 0.280 10 43113628 missense variant G/A;C;T snv 1
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 1
rs377767432
RET
0.925 0.160 10 43121980 missense variant C/A;T snv 1
rs55947360
RET
1.000 0.120 10 43119669 missense variant G/A;T snv 4.0E-05; 4.0E-06 1
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 1
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 1
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 1