rs371638091, None

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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 12 120920824 downstream gene variant TT/-;T;TTT delins 0.33 0.700 1.000 1 2016 2016
Finding of Mean Corpuscular Hemoglobin
1206 12 120920824 downstream gene variant TT/-;T;TTT delins 0.33 0.700 1.000 1 2016 2016