Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 5
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs8176644
ABO
9 133273734 intron variant C/T snv 4
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 4
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins 4
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11 4
rs8176643
ABO
9 133274294 intron variant C/- del 3
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11 3
rs643434
ABO
9 133266942 intron variant A/G;T snv 3
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15 3
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 2
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv 2
rs10793962
ABO
9 133253728 non coding transcript exon variant A/T snv 0.11 2
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 2
rs8176720
ABO
9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 2