rs760370, SLC29A1

N. diseases: 3
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.
Anemia
CUI: C0002871
Disease: Anemia
94 0.925 0.120 6 44233216 intron variant A/G snv 0.36 0.030 0.333 3 2015 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.925 0.120 6 44233216 intron variant A/G snv 0.36 0.010 1.000 1 2017 2017
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.925 0.120 6 44233216 intron variant A/G snv 0.36 0.010 1.000 1 2016 2016