rs2231137, ABCG2

N. diseases: 13
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.
URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1
2 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.700 0
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.030 1.000 3 2007 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.020 1.000 2 2009 2018
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2008 2008
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2009 2009
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2015 2015
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2016 2016
Gout
CUI: C0018099
Disease: Gout
2354 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2014 2014
gout tophaceous
CUI: C0744466
Disease: gout tophaceous
3 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2014 2014
Heart Septal Defects
CUI: C0018816
Disease: Heart Septal Defects
12 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2014 2014
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2019 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1.000 1 2018 2018
Skin toxicity
CUI: C1167791
Disease: Skin toxicity
24 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 0.010 1 2018 2018