Gene: ABO ×
Source: ALL
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 2 2018 2019
dbSNP: rs10793962
rs10793962
ABO
2 9 133253728 non coding transcript exon variant A/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs115478735
rs115478735
ABO
1 9 133274295 intron variant A/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs139840563
rs139840563
ABO
1 9 133271018 intron variant -/GACAA;GACAAGACAA delins 0.700 1.000 1 2018 2018
dbSNP: rs149037075
rs149037075
ABO
3 9 133255469 3 prime UTR variant CTGT/- delins 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2519093
rs2519093
ABO
16 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs35230453
rs35230453
ABO
1 9 133266030 intron variant AA/-;A;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAAAAA delins 0.700 1.000 1 2018 2018
dbSNP: rs492488
rs492488
ABO
3 9 133269548 intron variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs550057
rs550057
ABO
11 0.925 0.080 9 133271182 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs587611953
rs587611953
ABO
1 9 133270004 intron variant C/A snv 0.700 1.000 1 2018 2018
dbSNP: rs587729126
rs587729126
ABO
1 9 133263363 intron variant CACCACTACGCC/- delins 0.700 1.000 1 2018 2018
dbSNP: rs676457
rs676457
ABO
3 1.000 0.120 9 133270797 intron variant T/A snv 0.700 1.000 1 2018 2018
dbSNP: rs687621
rs687621
ABO
18 0.851 0.240 9 133261662 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs8176643
rs8176643
ABO
3 9 133274294 intron variant C/- del 0.700 1.000 1 2018 2018
dbSNP: rs8176672
rs8176672
ABO
2 1.000 0.040 9 133266772 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs8176693
rs8176693
ABO
9 0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 0.700 1.000 1 2018 2018
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 2018 2018
dbSNP: rs8176746
rs8176746
ABO
12 0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 0.700 1.000 1 2018 2018
dbSNP: rs8176747
rs8176747
ABO
6 9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 0.700 1.000 1 2018 2018
dbSNP: rs9411377
rs9411377
ABO
2 9 133269992 intron variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs9411378
rs9411378
ABO
5 9 133270015 intron variant A/C;T snv 0.700 1.000 1 2018 2018