rs422982, SLC11A2

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.
Childhood Acute Lymphoblastic Leukemia
261 0.925 0.200 12 51012571 intron variant T/A;C snv 0.010 1.000 1 2014 2014
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.925 0.200 12 51012571 intron variant T/A;C snv 0.010 1.000 1 2014 2014