rs104893662, SLC40A1

N. diseases: 4
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, TYPE 4
CUI: C1853733
Disease: HEMOCHROMATOSIS, TYPE 4
26 0.851 0.080 2 189571799 missense variant T/A;G snv 0.800 1.000 13 2000 2005
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.851 0.080 2 189571799 missense variant T/A;G snv 0.010 1.000 1 2003 2003
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.851 0.080 2 189571799 missense variant T/A;G snv 0.010 1.000 1 2003 2003
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.851 0.080 2 189571799 missense variant T/A;G snv 0.010 1.000 1 2003 2003