rs35947132, PRF1

N. diseases: 10
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.
Familial Hemophagocytic Lymphocytosis
CUI: C0272199
Disease: Familial Hemophagocytic Lymphocytosis
6 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.040 1.000 4 2005 2008
Lymphohistiocytosis, Hemophagocytic
CUI: C0024291
Disease: Lymphohistiocytosis, Hemophagocytic
13 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.020 1.000 2 2005 2014
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2015 2015
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2006 2006
Latent Tuberculosis
CUI: C1609538
Disease: Latent Tuberculosis
18 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2006 2006
leukemia
CUI: C0023418
Disease: leukemia
144 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2013 2013
Macrophage Activation Syndrome
CUI: C1096155
Disease: Macrophage Activation Syndrome
6 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2008 2008
Systemic onset juvenile chronic arthritis
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
53 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2010 2010
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.776 0.280 10 70600631 missense variant G/A snv 2.9E-02 2.9E-02 0.010 1.000 1 2006 2006