Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs794728625
MEN1
1.000 0.120 11 64807228 intron variant C/T snv 1
rs104894261
MAP4K2 ; MEN1
1.000 0.120 11 64804588 stop gained G/A 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
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
rs750904332
MEN1
1.000 0.120 11 64806312 stop gained G/A;C;T snv 4.0E-06 2
rs794728615
MEN1
0.882 0.160 11 64810025 stop gained G/A;C snv 4.2E-06 2
rs794728631
MEN1 ; MAP4K2
1.000 0.120 11 64804507 stop gained G/A snv 2
rs794728647
MEN1
1.000 0.120 11 64809788 stop gained G/A;C snv 8.0E-06 2
rs863224526
MEN1 ; MAP4K2
1.000 0.120 11 64804738 stop gained C/A;G snv 2
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
rs104894260
MEN1 ; MAP4K2
1.000 0.120 11 64805077 stop gained C/T snv 1
rs104894265
MEN1
1.000 0.120 11 64805758 stop gained G/T snv 1
rs1057520733
MEN1
1.000 0.120 11 64807554 stop gained G/A snv 1
rs1060499987
MEN1
1.000 0.120 11 64809792 stop gained A/T snv 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
rs141679530
MEN1 ; MAP4K2
1.000 0.120 11 64804632 stop gained G/A;C;T snv 3.4E-05 1
rs1555166365
MEN1
1.000 0.120 11 64809732 stop gained C/T snv 1
rs1555166567
MEN1
1.000 0.120 11 64809879 stop gained G/C snv 1
rs1565647197
MEN1
1.000 0.120 11 64807676 stop gained C/T snv 1
rs1565647767
MEN1
1.000 0.120 11 64807920 stop gained G/A snv 1