rs116855232, NUDT15

N. diseases: 12
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.
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.800 1.000 26 2014 2020
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.750 1.000 7 2016 2019
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.750 1.000 5 2016 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.730 1.000 4 2014 2018
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.020 1.000 2 2015 2016
Agranulocytosis
CUI: C0001824
Disease: Agranulocytosis
8 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2018 2018
Alopecia totalis
CUI: C0263504
Disease: Alopecia totalis
1 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2016 2016
Childhood Acute Lymphoblastic Leukemia
261 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2017 2017
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2016 2016
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2018 2018
Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2016 2016
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2018 2018