Disease: Medullary carcinoma of thyroid
Source: ALL
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-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 29
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 17
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 15
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 14
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
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
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 9
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
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs34682185
RET
0.851 0.120 10 43106382 missense variant G/A snv 6.3E-04 2.2E-04 4