Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867966048 1.000 0.080 1 161340637 missense variant G/A;C snv 2
rs104886028 1.000 0.080 12 25227308 missense variant C/T snv 1
rs121913309
RET
1.000 0.080 10 43120164 inframe deletion TGTTTATGAAGA/- delins 1
rs121913312
RET
1.000 0.080 10 43114494 inframe deletion GAGCTG/- del 1
rs121913313
RET
1.000 0.080 10 43113626 inframe deletion TTCCCTGAGGAGGAGAAGTGCTTCTGC/- delins 1
rs3026785
RET
1.000 0.080 10 43130238 3 prime UTR variant T/C snv 4.3E-02 1
rs9282655 1.000 0.080 16 68823545 missense variant T/C snv 1
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs769177037 1.000 0.080 1 161328467 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 1
rs864622088 0.925 0.080 9 95459774 missense variant G/T snv 4.0E-06 2
rs377767415
RET
0.925 0.120 10 43118418 missense variant A/G snv 4.0E-06 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs75030001
RET
0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 7
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs145633958
RET
1.000 0.080 10 43100551 missense variant C/A;T snv 2.7E-03; 4.0E-06 1
rs146838520
RET
0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 4
rs377767427
RET
0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06 3
rs750371239
ATM
1.000 0.080 11 108252912 missense variant G/A snv 4.0E-06 1
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 17
rs773631693
RET
1.000 0.080 10 43106436 missense variant C/A snv 4.0E-06 1
rs770599902 1.000 0.080 1 161362382 missense variant G/A snv 4.0E-06 1
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 15
rs777122776
RET
1.000 0.080 10 43114515 missense variant G/A;T snv 2.8E-05; 4.0E-06 1
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21