Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 2
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 2
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 2
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 2
rs397507511
PTPN11
0.882 0.240 12 112450385 missense variant G/A;C snv 2
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 2
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 2
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 1
rs121918465
PTPN11
0.827 0.200 12 112450407 missense variant A/C;G;T snv 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs121918468
PTPN11
0.882 0.160 12 112488444 missense variant G/A;T snv 1
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 1
rs397509345
PTPN11
0.851 0.160 12 112489093 missense variant AG/CC mnv 1
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 1
rs397507541
PTPN11
0.827 0.160 12 112489068 missense variant C/T snv 4.0E-06 7.0E-06 1
rs121918469
PTPN11
0.882 0.160 12 112488454 missense variant G/C snv 1
rs397507542
PTPN11
0.790 0.320 12 112489069 missense variant G/T snv 1
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 1
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 1
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 1
rs397507543
PTPN11
0.925 0.160 12 112489078 missense variant G/A snv 1
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 1
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 1
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 1