Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
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
rs2066827
GPR19 ; CDKN1B
0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 14
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs146838520
RET
0.851 0.120 10 43120129 missense variant C/T snv 4.0E-06 2.8E-05 4
rs775984846
NTRK1
1.000 1 156881535 missense variant G/A;C snv 3.5E-05 2
rs2245020
GFRA1
1.000 10 116125439 missense variant G/A;C snv 0.57 1
rs1490900384
GFRA2
1.000 8 21705094 synonymous variant G/A snv 4.1E-06 1
rs1293540396
NTRK1
1.000 1 156868557 synonymous variant C/T snv 1.8E-05 2.8E-05 1