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: rs2519093
rs2519093
ABO
14 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 2 2015 2018
dbSNP: rs507666
rs507666
ABO
6 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 2 2017 2018