Gene: PTPN11 ×
Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397507510
rs397507510
PTPN11
5 0.776 0.280 12 112450361 missense variant G/A;C;T snv 0.700 1.000 28 2002 2016
dbSNP: rs121918455
rs121918455
PTPN11
31 0.695 0.440 12 112477720 missense variant A/C;G snv 0.700 1.000 14 2003 2009
dbSNP: rs121918454
rs121918454
PTPN11
16 0.742 0.280 12 112450395 missense variant C/A;G;T snv 0.700 1.000 11 2003 2016
dbSNP: rs397507512
rs397507512
PTPN11
2 0.925 0.160 12 112450391 missense variant T/C;G snv 0.700 1.000 10 2003 2016
dbSNP: rs397507549
rs397507549
PTPN11
6 0.742 0.240 12 112489104 missense variant C/A;G snv 0.700 1.000 9 2006 2015
dbSNP: rs397507531
rs397507531
PTPN11
18 0.752 0.320 12 112473040 missense variant T/C;G snv 0.700 1.000 8 2003 2009
dbSNP: rs397507506
rs397507506
PTPN11
6 0.807 0.240 12 112450354 missense variant C/A;G snv 0.700 1.000 7 2003 2015
dbSNP: rs397516810
rs397516810
PTPN11
2 0.925 0.160 12 112477652 missense variant T/G snv 0.700 1.000 7 2002 2014
dbSNP: rs121918470
rs121918470
PTPN11
10 0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 0.700 1.000 6 2004 2012
dbSNP: rs727503380
rs727503380
PTPN11
2 0.925 0.160 12 112450386 missense variant A/T snv 0.700 1.000 6 2004 2013
dbSNP: rs121918468
rs121918468
PTPN11
3 0.882 0.160 12 112488444 missense variant G/A;T snv 0.700 1.000 5 2004 2013
dbSNP: rs121918459
rs121918459
PTPN11
46 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 0.700 1.000 3 2002 2006
dbSNP: rs397507518
rs397507518
PTPN11
2 0.925 0.160 12 112450508 missense variant G/A snv 0.700 1.000 2 2014 2014
dbSNP: rs121918453
rs121918453
PTPN11
15 0.732 0.280 12 112450394 missense variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs121918466
rs121918466
PTPN11
12 0.752 0.280 12 112450416 missense variant A/G snv 0.700 0
dbSNP: rs397507520
rs397507520
PTPN11
34 0.658 0.520 12 112453279 missense variant G/C;T snv 0.700 0