Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894256
MEN1
1.000 0.120 11 64810045 missense variant A/C snv 1
rs104894257
MEN1
1.000 0.120 11 64807951 stop gained C/T snv 1
rs104894258
MEN1
1.000 0.120 11 64807952 stop gained C/T snv 1
rs104894259
MAP4K2 ; MEN1
1.000 0.120 11 64805078 missense variant A/G;T snv 2
rs104894260
MEN1 ; MAP4K2
1.000 0.120 11 64805077 stop gained C/T snv 1
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
rs104894265
MEN1
1.000 0.120 11 64805758 stop gained G/T snv 1
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
rs1057520733
MEN1
1.000 0.120 11 64807554 stop gained G/A snv 1
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
rs1060499981
MEN1 ; MAP4K2
1.000 0.120 11 64805056 missense variant G/T snv 1
rs1060499986
MEN1 ; MAP4K2
1.000 0.120 11 64804818 splice acceptor variant T/C snv 1
rs1060499987
MEN1
1.000 0.120 11 64809792 stop gained A/T snv 1
rs1060499990
MEN1
1.000 0.120 11 64809942 frameshift variant G/- delins 1
rs1060499991
MAP4K2 ; MEN1
1.000 0.120 11 64804755 stop gained C/T snv 1
rs1060499992
MEN1
1.000 0.120 11 64809764 stop gained C/A;T snv 1
rs1060503789
MEN1
1.000 0.120 11 64807095 stop gained G/A;T snv 4.0E-06 2
rs1114167469
MEN1
0.925 0.160 11 64806322 missense variant G/A snv 1
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