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: rs10793962
rs10793962
ABO
2 9 133253728 non coding transcript exon variant A/T snv 0.11 0.700 1.000 2 2018 2018
dbSNP: rs8176741
rs8176741
ABO
1 9 133256074 synonymous variant G/A snv 0.12 0.11 0.700 1.000 2 2017 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 2017 2017
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 2014 2014
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