Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 9
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
rs104894263
MEN1
1.000 0.120 11 64809695 missense variant G/C snv 2
rs104894264
MEN1 ; MAP4K2
1.000 0.120 11 64805132 missense variant C/A;G;T snv 2
rs104894266
MEN1
1.000 0.120 11 64807557 stop gained G/A snv 2
rs104894267
MEN1 ; MAP4K2
1.000 0.120 11 64804789 stop gained G/A;T snv 7.0E-06 2
rs1060499974
MEN1 ; MAP4K2
1.000 0.120 11 64805141 stop gained G/A snv 7.0E-06 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
rs1114167486
MEN1
1.000 0.120 11 64809873 frameshift variant G/- delins 2
rs1114167489
MEN1
1.000 0.120 11 64806231 splice donor variant C/G;T snv 2
rs1114167498
MEN1
1.000 0.120 11 64806370 splice acceptor variant T/C snv 2
rs1114167524
MAP4K2 ; MEN1
1.000 0.120 11 64805159 frameshift variant -/GGAC ins 2
rs1114167528
MEN1 ; MAP4K2
1.000 0.120 11 64805103 missense variant A/T snv 2
rs1114167531
MEN1 ; MAP4K2
1.000 0.120 11 64804777 frameshift variant -/CTCTCGGC delins 2
rs1114167536
MEN1 ; MAP4K2
1.000 0.120 11 64804753 frameshift variant -/ACGGCTCC delins 2
rs1555165488
MEN1
0.925 0.120 11 64807566 frameshift variant -/AGCTCCA delins 2
rs376872829
MEN1
1.000 0.120 11 64808019 missense variant C/A;G;T snv 2.0E-05; 4.0E-06 2
rs386134249
MEN1 ; MAP4K2
1.000 0.120 11 64805122 missense variant C/T snv 2
rs386134250
MEN1
1.000 0.120 11 64810109 start lost T/A;C;G snv 2
rs397515385
MEN1
1.000 0.120 11 64809708 frameshift variant G/- del 2