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.
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
220 11 5805773 intron variant T/C snv 0.11 0.700 1.000 1 2008 2008
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 11 5805773 intron variant T/C snv 0.11 0.700 1.000 1 2016 2016