rs10901252, ABO

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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 9 133252613 non coding transcript exon variant G/C snv 0.11 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 9 133252613 non coding transcript exon variant G/C snv 0.11 0.700 1.000 1 2016 2016
von Willebrand's factor (lab test)
CUI: C2239219
Disease: von Willebrand's factor (lab test)
427 9 133252613 non coding transcript exon variant G/C snv 0.11 0.700 1.000 1 2019 2019