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 0.700 1.000 1 2013 2013
dbSNP: rs514659
rs514659
ABO
10 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs529565
rs529565
ABO
13 0.851 0.120 9 133274084 intron variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs545971
rs545971
ABO
8 9 133267960 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs612169
rs612169
ABO
10 9 133268030 intron variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs643434
rs643434
ABO
8 9 133266942 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs644234
rs644234
ABO
7 9 133266804 intron variant G/T snv 0.700 1.000 1 2013 2013
dbSNP: rs657152
rs657152
ABO
22 0.882 0.200 9 133263862 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs674302
rs674302
ABO
8 9 133271249 intron variant A/T snv 0.700 1.000 1 2013 2013
dbSNP: rs687289
rs687289
ABO
15 1.000 0.120 9 133261703 intron variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs687621
rs687621
ABO
18 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2013 2013