Source: CLINVAR ×
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 17
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 14
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 11
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 10
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 10
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 9
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 9
rs77503355
RET
0.776 0.160 10 43113655 missense variant G/A;C;T snv 8
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 8
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 8
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 8
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 7
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 6
rs377767429
RET
0.790 0.120 10 43120120 missense variant GC/TT mnv 5
rs587776841
MEN1
0.925 0.120 11 64809858 frameshift variant ACAG/- delins 3
rs104894259
MAP4K2 ; MEN1
1.000 0.120 11 64805078 missense variant A/G;T snv 2
rs104894261
MAP4K2 ; MEN1
1.000 0.120 11 64804588 stop gained G/A snv 2
rs1114167524
MAP4K2 ; MEN1
1.000 0.120 11 64805159 frameshift variant -/GGAC ins 2
rs767319284
MAP4K2 ; MEN1
1.000 0.120 11 64804621 frameshift variant G/-;GG delins 2
rs863224527
MAP4K2 ; MEN1
1.000 0.120 11 64804503 missense variant C/T snv 2
rs104894263
MEN1
1.000 0.120 11 64809695 missense variant G/C snv 2
rs104894266
MEN1
1.000 0.120 11 64807557 stop gained G/A snv 2
rs1060499976
MEN1
1.000 0.120 11 64807178 splice donor variant C/A;G;T snv 2
rs1060503789
MEN1
1.000 0.120 11 64807095 stop gained G/A;T snv 4.0E-06 2
rs1114167482
MEN1
1.000 0.120 11 64806259 stop gained C/T snv 2