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: rs507666
rs507666
ABO
8 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 4 2013 2019
dbSNP: rs550057
rs550057
ABO
11 0.925 0.080 9 133271182 intron variant T/A;C snv 0.700 1.000 3 2015 2019
dbSNP: rs2519093
rs2519093
ABO
16 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 2 2018 2018
dbSNP: rs630014
rs630014
ABO
9 9 133274306 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs9411378
rs9411378
ABO
5 9 133270015 intron variant A/C;T snv 0.700 1.000 1 2018 2018