rs779021719, HAMP

N. diseases: 5
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 2B
CUI: C1865616
Disease: HEMOCHROMATOSIS, TYPE 2B
5 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 0.700 1.000 5 2003 2004
Hepatic siderosis
CUI: C0948120
Disease: Hepatic siderosis
1 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 0.010 1.000 1 2015 2015
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 0.010 1.000 1 2011 2011
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 0.010 1.000 1 2011 2011
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 0.010 1.000 1 2015 2015