Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 22
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
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
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
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
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
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 6
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 6
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 5
rs794728615
MEN1
0.882 0.160 11 64810025 stop gained G/A;C snv 4.2E-06 4
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 4
rs145047094
AIP
0.882 0.160 11 67483205 missense variant G/A snv 2.0E-03 1.9E-03 3
rs149383809
MEN1
0.925 0.120 11 64805722 missense variant T/A snv 7.2E-05 3.5E-05 2
rs760629445
MEN1
0.925 0.120 11 64810048 missense variant C/A;T snv 4.2E-06; 8.4E-06 2
rs794728648
MEN1
0.925 0.120 11 64808078 missense variant C/A;T snv 2
rs1060499991
MAP4K2 ; MEN1
1.000 0.120 11 64804755 stop gained C/T snv 1
rs104894263
MEN1
1.000 0.120 11 64809695 missense variant G/C snv 1
rs1114167469
MEN1
0.925 0.160 11 64806322 missense variant G/A snv 1
rs1114167494
MEN1
1.000 0.120 11 64808031 missense variant C/A snv 1