rs779359707, TFRC

N. diseases: 2
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 0.925 0.080 3 196073990 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.925 0.080 3 196073990 missense variant T/C snv 4.0E-06 0.010 1.000 1 2008 2008