Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1420960657 0.851 0.080 11 112093192 missense variant A/G snv 4
rs62624461 0.851 0.080 7 97117880 missense variant T/C snv 2.0E-02 1.8E-02 4
rs377767430
RET
0.882 0.080 10 43120192 missense variant A/C;G snv 3
rs79661516
RET
0.882 0.080 10 43105018 missense variant G/A snv 3
rs942160050 0.882 0.080 1 161356685 missense variant C/A;G;T snv 4.0E-06 3
rs374918502 0.925 0.080 1 156880056 missense variant C/T snv 6.0E-05 7.6E-06 2
rs869025630
VHL
0.925 0.080 3 10142158 missense variant G/C;T snv 2
rs876659313
VHL
0.925 0.080 3 10146624 missense variant A/C;G snv 2
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 15
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 9
rs146646971
RET
0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 7
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T snv 5
rs34682185
RET
0.851 0.120 10 43106382 missense variant G/A snv 6.3E-04 2.2E-04 4
rs377767402
RET
0.882 0.120 10 43113663 missense variant G/A snv 2.4E-05 2.8E-05 4
rs55846256
RET
0.882 0.120 10 43114493 missense variant C/A;T snv 4.0E-06; 1.3E-04 4
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
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
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 8
rs1416313401 0.827 0.160 8 109578004 missense variant A/G snv 4.1E-06 5
rs1183365192
RET
0.851 0.160 10 43106550 missense variant C/T snv 7.0E-06 4
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs1060503770 0.851 0.200 11 112094815 stop gained C/G;T snv 4.0E-06 5