Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs377767394
RET
0.925 0.080 10 43113603 missense variant A/C snv 2
rs143795581
RET
0.851 0.120 10 43114596 missense variant A/C;G snv 8.0E-06 5
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs11214077
SDHD ; TIMM8B
0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs1188536960
SORD
0.882 0.120 15 45043305 missense variant A/G snv 5
rs377767442
RET
0.827 0.160 10 43121967 missense variant A/G snv 5
rs377767395
RET
0.882 0.120 10 43113613 missense variant A/G snv 4
rs377767415
RET
0.925 0.120 10 43118418 missense variant A/G snv 4.0E-06 2
rs33927012
SDHB
1.000 0.080 1 17027802 missense variant A/G snv 1.2E-02 9.3E-03 1
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs121913306
RET
0.851 0.120 10 43120119 missense variant AGC/TTT mnv 4
rs773631693
RET
1.000 0.080 10 43106436 missense variant C/A snv 4.0E-06 1
rs1800863
RET
0.851 0.160 10 43120185 synonymous variant C/A;G snv 1.6E-05; 0.21 4
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
rs145633958
RET
1.000 0.080 10 43100551 missense variant C/A;T snv 2.7E-03; 4.0E-06 1
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs377767427
RET
0.882 0.120 10 43120114 missense variant C/G snv 4.0E-06 3
rs377767426
RET
1.000 0.080 10 43119694 missense variant C/G snv 1.8E-04 1.0E-04 2
rs146838520
RET
0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 4
rs148935214
RET
0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 3
rs104886028
KRAS
1.000 0.080 12 25227308 missense variant C/T snv 1
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11