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: rs8176746
rs8176746
ABO
12 0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 0.800 1.000 2 2010 2012
dbSNP: rs8176749
rs8176749
ABO
7 1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 0.800 1.000 2 2012 2018
dbSNP: rs2073824
rs2073824
ABO
2 9 133257246 intron variant A/G snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs514659
rs514659
ABO
10 0.882 0.120 9 133266790 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs529565
rs529565
ABO
13 0.851 0.120 9 133274084 intron variant C/T snv 0.700 1.000 1 2012 2012
dbSNP: rs545971
rs545971
ABO
8 9 133267960 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs612169
rs612169
ABO
10 9 133268030 intron variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 9 133274306 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs674302
rs674302
ABO
8 9 133271249 intron variant A/T snv 0.700 1.000 1 2012 2012
dbSNP: rs687621
rs687621
ABO
18 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7853989
rs7853989
ABO
2 9 133256205 missense variant G/A;C snv 1.2E-05; 0.13 0.700 1.000 1 2012 2012
dbSNP: rs8176644
rs8176644
ABO
4 9 133273734 intron variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs8176693
rs8176693
ABO
9 0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs8176720
rs8176720
ABO
3 9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 0.700 1.000 1 2012 2012
dbSNP: rs8176722
rs8176722
ABO
3 1.000 0.040 9 133257367 intron variant C/A snv 0.13 0.12 0.700 1.000 1 2012 2012
dbSNP: rs8176725
rs8176725
ABO
2 9 133257230 intron variant G/A snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs8176730
rs8176730
ABO
2 9 133257138 intron variant T/C snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs8176731
rs8176731
ABO
1 9 133256963 intron variant T/C snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs8176743
rs8176743
ABO
7 1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 0.700 1.000 1 2012 2012
dbSNP: rs8176747
rs8176747
ABO
6 9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 0.700 1.000 1 2012 2012