Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs1555166368
MEN1
0.851 0.120 11 64809738 frameshift variant GA/- del 6
rs2959656
MEN1 ; MAP4K2
0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90 5
rs121908260
INS ; INS-IGF2
0.851 0.160 11 2160835 missense variant C/T snv 4
rs193920817
TP53
0.925 0.160 17 7675131 missense variant C/T snv 3
rs386834266
MIR6764 ; YY1
1.000 0.120 14 100277470 missense variant C/G snv 2
rs749317102
LOC101929532 ; GCG
1.000 0.120 2 162147470 missense variant T/C snv 1.2E-05 7.0E-06 1
rs730882000
TP53
1.000 0.120 17 7675137 missense variant C/G;T snv 1