rs397507546, PTPN11

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Juvenile Myelomonocytic Leukemia
CUI: C0349639
Disease: Juvenile Myelomonocytic Leukemia
70 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 2 2003 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Leopard Syndrome 1
CUI: C4551484
Disease: Leopard Syndrome 1
26 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.700 0
Histiocytic sarcoma
CUI: C0334663
Disease: Histiocytic sarcoma
8 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.360 12 112489084 missense variant G/A;C;T snv 0.010 1 2019 2019