Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
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
rs77316810
RET
0.776 0.200 10 43113654 missense variant T/A;C;G snv 10
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
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 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
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
rs377767395
RET
0.882 0.120 10 43113613 missense variant A/G snv 4
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