rs199474387, HLA-A

N. diseases: 6
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 0.807 0.240 6 29942870 missense variant G/C;T snv 0.030 1.000 3 1998 2002
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.807 0.240 6 29942870 missense variant G/C;T snv 0.020 1.000 2 1998 2002
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.807 0.240 6 29942870 missense variant G/C;T snv 0.020 1.000 2 1998 2002
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.807 0.240 6 29942870 missense variant G/C;T snv 0.010 1.000 1 2002 2002
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.807 0.240 6 29942870 missense variant G/C;T snv 0.010 1.000 1 2002 2002
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.807 0.240 6 29942870 missense variant G/C;T snv 0.010 1 1998 1998