Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 3
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs794728648
MEN1
0.925 0.120 11 64808078 missense variant C/A;T snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 2
rs104894259
MAP4K2 ; MEN1
1.000 0.120 11 64805078 missense variant A/G;T snv 1
rs863224527
MAP4K2 ; MEN1
1.000 0.120 11 64804503 missense variant C/T snv 1
rs104894256
MEN1
1.000 0.120 11 64810045 missense variant A/C snv 1
rs104894263
MEN1
1.000 0.120 11 64809695 missense variant G/C snv 1
rs1057521110
MEN1
1.000 0.120 11 64807662 missense variant C/T snv 1
rs1064793167
MEN1
1.000 0.120 11 64808010 missense variant C/T snv 1
rs1114167469
MEN1
0.925 0.160 11 64806322 missense variant G/A snv 1
rs1114167491
MEN1
1.000 0.120 11 64809977 missense variant C/T snv 1
rs1114167493
MEN1
1.000 0.120 11 64807082 missense variant C/T snv 1
rs1114167494
MEN1
1.000 0.120 11 64808031 missense variant C/A snv 1
rs1114167495
MEN1
1.000 0.120 11 64806331 missense variant T/C snv 1
rs1114167515
MEN1
1.000 0.120 11 64809694 missense variant T/C snv 1
rs1114167543
MEN1
1.000 0.120 11 64809680 missense variant A/C snv 1
rs1298484645
MEN1
1.000 0.120 11 64805666 missense variant G/A snv 4.0E-06 1
rs1389398299
MEN1
1.000 0.120 11 64809781 missense variant C/G;T snv 8.0E-06 1