Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs377767397
RET
0.790 0.280 10 43113628 missense variant G/A;C;T snv 10
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs77316810
RET
0.776 0.200 10 43113654 missense variant T/A;C;G snv 10
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 9
rs377767398
RET
0.807 0.280 10 43113628 missense variant GC/AT;CT;TT mnv 8
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 8
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 8
rs146646971
RET
0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 7
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 7
rs75030001
RET
0.807 0.160 10 43118458 missense variant G/C;T snv 4.0E-06; 2.0E-05 7
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs143795581
RET
0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06 5
rs377767391
RET
0.827 0.160 10 43113627 missense variant T/A;C;G snv 5
rs377767442
RET
0.827 0.160 10 43121967 missense variant A/G snv 5
rs121913306
RET
0.851 0.120 10 43120119 missense variant AGC/TTT mnv 4
rs146838520
RET
0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 4
rs1800863
RET
0.851 0.160 10 43120185 synonymous variant C/A;G snv 1.6E-05; 0.21 4
rs34682185
RET
0.851 0.120 10 43106382 missense variant G/A snv 6.3E-04 2.2E-04 4
rs377767395
RET
0.882 0.120 10 43113613 missense variant A/G snv 4
rs148935214
RET
0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 3
rs377767427
RET
0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06 3
rs78347871
RET
0.882 0.120 10 43121950 missense variant G/A;C;T snv 8.0E-06; 2.0E-05 3
rs2075912
RET
0.925 0.160 10 43126769 3 prime UTR variant T/C snv 0.79 0.84 2