rs11568350, SLC40A1

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.
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.020 1.000 2 2004 2007
Anemia
CUI: C0002871
Disease: Anemia
94 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2004 2004
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2007 2007
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2007 2007
HIV Infections
CUI: C0019693
Disease: HIV Infections
142 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2012 2012
Human herpesvirus 8 infection
CUI: C1512508
Disease: Human herpesvirus 8 infection
2 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2016 2016
Opportunistic Infections
CUI: C0029118
Disease: Opportunistic Infections
7 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2012 2012
Pneumocystis jiroveci pneumonia
CUI: C1535939
Disease: Pneumocystis jiroveci pneumonia
5 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2012 2012
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 0.010 1.000 1 2012 2012