Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 21
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 21
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 21
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 19
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 18
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 17
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 16
rs11214077
SDHD ; TIMM8B
0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 11
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 11
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 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 9
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 8
rs377767397
RET
0.790 0.280 10 43113628 missense variant G/A;C;T snv 7
rs377767398
RET
0.807 0.280 10 43113628 missense variant GC/AT;CT;TT mnv 7
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 7
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 6