rs676996, ABO

N. diseases: 1
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.
Glycine measurement
CUI: C0523677
Disease: Glycine measurement
68 9 133270647 intron variant G/T snv 0.700 1.000 1 2019 2019