rs1142345, TPMT

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.
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.700 1.000 1 2017 2017
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.030 1.000 3 2008 2013
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.030 1.000 3 2008 2013
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.030 1.000 3 2008 2013
Thiopurine S methyltranferase deficiency
CUI: C0342801
Disease: Thiopurine S methyltranferase deficiency
4 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.020 1.000 2 2004 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.010 1.000 1 2006 2006
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.010 1.000 1 2006 2006
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.010 1.000 1 2006 2006
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 0.010 1.000 1 2006 2006