Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 24
rs121918467
PTPN11
0.807 0.280 12 112486482 missense variant C/A;T snv 8.0E-06; 1.2E-05 23
rs397507545
PTPN11
0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs397507531
PTPN11
0.752 0.320 12 112473040 missense variant T/C;G snv 18
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 17
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 15
rs121918466
PTPN11
0.752 0.280 12 112450416 missense variant A/G snv 14
rs397507547
PTPN11
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06 14
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 9
rs397507542
PTPN11
0.790 0.320 12 112489069 missense variant G/T snv 9
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 9
rs121918458
PTPN11
0.807 0.320 12 112489080 missense variant T/A;G snv 8