Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs8176704
rs8176704
ABO
5 0.925 0.080 9 133260148 intron variant G/A snv 0.010 1.000 1 2015 2015