rs1275561861, HLA-A

N. diseases: 23
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.
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.672 0.360 6 29944350 missense variant G/A snv 0.100 0.923 13 1998 2017
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.672 0.360 6 29944350 missense variant G/A snv 0.090 0.889 9 2001 2017
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.672 0.360 6 29944350 missense variant G/A snv 0.080 1.000 8 1997 2013
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.672 0.360 6 29944350 missense variant G/A snv 0.060 0.833 6 2004 2013
Childhood Acute Lymphoblastic Leukemia
261 0.672 0.360 6 29944350 missense variant G/A snv 0.020 1.000 2 2002 2013
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
85 0.672 0.360 6 29944350 missense variant G/A snv 0.020 1.000 2 2004 2005
IgG Deficiency disorder
CUI: C0162539
Disease: IgG Deficiency disorder
2 0.672 0.360 6 29944350 missense variant G/A snv 0.020 1.000 2 2004 2005
Acquired Hypogammaglobulinemia
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
4 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2004 2004
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2013 2013
Adult Acute Lymphocytic Leukemia
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
154 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2013 2013
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2002 2002
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2002 2002
Chronic viral hepatitis
CUI: C0276623
Disease: Chronic viral hepatitis
8 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
leukemia
CUI: C0023418
Disease: leukemia
144 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2002 2002
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2004 2004
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2014 2014
Portal Hypertension
CUI: C0020541
Disease: Portal Hypertension
9 0.672 0.360 6 29944350 missense variant G/A snv 0.010 1.000 1 2009 2009