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: rs62574565
rs62574565
ABO
1 9 133252872 non coding transcript exon variant G/A snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs58081338
rs58081338
ABO
1 9 133252942 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs62574567
rs62574567
ABO
1 9 133253034 non coding transcript exon variant C/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs7857390
rs7857390
ABO
2 9 133253159 non coding transcript exon variant A/G snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs12554336
rs12554336
ABO
1 9 133253276 non coding transcript exon variant A/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs12554339
rs12554339
ABO
1 9 133253350 non coding transcript exon variant A/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs10901253
rs10901253
ABO
1 9 133253385 non coding transcript exon variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs11244052
rs11244052
ABO
1 9 133253738 non coding transcript exon variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs11244053
rs11244053
ABO
1 9 133253973 non coding transcript exon variant A/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4962114
rs4962114
ABO
1 9 133254224 non coding transcript exon variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4962116
rs4962116
ABO
1 9 133254329 non coding transcript exon variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs8176748
rs8176748
ABO
2 9 133255902 missense variant C/A;T snv 4.0E-06; 0.27 0.700 1.000 1 2012 2012
dbSNP: rs8176742
rs8176742
ABO
1 9 133256050 synonymous variant C/T snv 0.24 0.22 0.700 1.000 1 2012 2012
dbSNP: rs7873635
rs7873635
ABO
1 9 133256625 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs8176726
rs8176726
ABO
1 9 133257221 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs8176715
rs8176715
ABO
1 9 133257761 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs8176714
rs8176714
ABO
4 9 133257791 intron variant G/A snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs4962040
rs4962040
ABO
1 9 133258141 intron variant G/A snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs641959
rs641959
ABO
4 9 133258308 intron variant A/C snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs641943
rs641943
ABO
4 9 133258323 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs514708
rs514708
ABO
4 9 133258352 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs626035
rs626035
ABO
4 9 133259603 intron variant T/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs547495
rs547495
ABO
1 9 133259604 intron variant T/C snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs8176702
rs8176702
ABO
1 9 133260743 intron variant G/A snv 0.700 1.000 1 2012 2012
dbSNP: rs2073826
rs2073826
ABO
1 9 133261560 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012