Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1555166368
MEN1
0.851 0.120 11 64809738 frameshift variant GA/- del 6
rs1188536960
SORD
0.882 0.120 15 45043305 missense variant A/G snv 5
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
rs1800863
RET
0.851 0.160 10 43120185 synonymous variant C/A;G snv 1.6E-05; 0.21 4
rs377767395
RET
0.882 0.120 10 43113613 missense variant A/G snv 4
rs377767427
RET
0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06 3
rs781609053
EGFR
0.925 0.120 7 55200379 missense variant T/C snv 1.2E-05 3
rs78347871
RET
0.882 0.120 10 43121950 missense variant G/A;C;T snv 8.0E-06; 2.0E-05 3
rs183334241
TSHZ1
0.925 0.080 18 75288186 missense variant G/A;C snv 1.6E-04 2
rs2565200
RET
0.925 0.160 10 43127485 3 prime UTR variant T/A;C snv 2
rs377767394
RET
0.925 0.080 10 43113603 missense variant A/C snv 2
rs377767414
RET
0.925 0.080 10 43118397 missense variant G/A snv 2
rs377767415
RET
0.925 0.120 10 43118418 missense variant A/G snv 4.0E-06 2
rs864622088
PTCH1
0.925 0.080 9 95459774 missense variant G/T snv 4.0E-06 2
rs867966048
SDHC
1.000 0.080 1 161340637 missense variant G/A;C snv 2
rs104886028
KRAS
1.000 0.080 12 25227308 missense variant C/T snv 1