Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 1
rs267606990
RPL6 ; PTPN11
0.851 0.240 12 112419116 missense variant C/T snv 1
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 1
rs397507506
PTPN11
0.807 0.240 12 112450354 missense variant C/A;G snv 1
rs397507509
PTPN11
0.807 0.240 12 112450359 missense variant G/C;T snv 1
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 2
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 2
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 1
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 1
rs397507511
PTPN11
0.882 0.240 12 112450385 missense variant G/A;C snv 2
rs121918453
PTPN11
0.732 0.280 12 112450394 missense variant G/A;C;T snv 2
rs121918454
PTPN11
0.742 0.280 12 112450395 missense variant C/A;G;T snv 2
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 1
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C 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
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 1
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 1
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 1
rs397507525
PTPN11
0.925 0.160 12 112472968 missense variant C/T snv 7.0E-06 1
rs376607329
PTPN11
0.851 0.200 12 112472981 missense variant G/A;T snv 3.2E-05 3.5E-05 1
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 2
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 1
rs397507531
PTPN11
0.752 0.320 12 112473040 missense variant T/C;G snv 1
rs121918463
PTPN11
0.851 0.240 12 112477651 missense variant T/A;C;G snv 1