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
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
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
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
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15 3
rs8176643
ABO
9 133274294 intron variant C/- del 3
rs10793962
ABO
9 133253728 non coding transcript exon variant A/T snv 0.11 2
rs492488
ABO
9 133269548 intron variant A/C;G;T snv 2
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 2
rs9411377
ABO
9 133269992 intron variant A/C snv 0.62 2
rs115478735
ABO
9 133274295 intron variant A/T snv 0.14 1
rs139840563
ABO
9 133271018 intron variant -/GACAA;GACAAGACAA delins 1
rs35230453
ABO
9 133266030 intron variant AA/-;A;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAAAAA delins 1
rs587611953
ABO
9 133270004 intron variant C/A snv 1
rs587729126
ABO
9 133263363 intron variant CACCACTACGCC/- delins 1
rs676457
ABO
1.000 0.120 9 133270797 intron variant T/A snv 1
rs8176672
ABO
1.000 0.040 9 133266772 intron variant C/G;T snv 1