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: rs687621
rs687621
ABO
18 0.851 0.240 9 133261662 intron variant G/A;C snv 0.800 1.000 2 2010 2013
dbSNP: rs2073825
rs2073825
ABO
3 9 133257320 intron variant A/T snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2073827
rs2073827
ABO
3 9 133261730 intron variant G/C snv 0.700 1.000 1 2013 2013
dbSNP: rs474279
rs474279
ABO
2 9 133264214 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs500498
rs500498
ABO
2 9 133273232 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: rs514708
rs514708
ABO
4 9 133258352 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs517414
rs517414
ABO
3 9 133258643 intron variant G/A snv 0.26 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: rs547643
rs547643
ABO
3 9 133259656 intron variant C/T snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs549331
rs549331
ABO
3 9 133259791 intron variant C/G snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs549446
rs549446
ABO
3 9 133259834 missense variant C/T snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs568203
rs568203
ABO
3 9 133276029 upstream gene variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs574347
rs574347
ABO
3 9 133260255 intron variant T/C snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs579483
rs579483
ABO
3 9 133260793 intron variant T/A snv 0.700 1.000 1 2013 2013
dbSNP: rs579622
rs579622
ABO
3 9 133260839 intron variant G/A snv 0.700 1.000 1 2013 2013
dbSNP: rs613423
rs613423
ABO
3 9 133260074 intron variant G/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs624601
rs624601
ABO
3 9 133259961 intron variant G/A snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs625593
rs625593
ABO
2 9 133259705 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs626035
rs626035
ABO
4 9 133259603 intron variant T/G snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs630014
rs630014
ABO
9 9 133274306 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs638756
rs638756
ABO
2 9 133259081 intron variant A/C snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs641943
rs641943
ABO
4 9 133258323 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs641959
rs641959
ABO
4 9 133258308 intron variant A/C snv 0.29 0.700 1.000 1 2013 2013