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: rs529565
rs529565
ABO
13 0.851 0.120 9 133274084 intron variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.020 < 0.001 2 2013 2017
dbSNP: rs2073824
rs2073824
ABO
2 9 133257246 intron variant A/G snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs8176668
rs8176668
ABO
2 9 133268647 intron variant A/T snv 0.010 < 0.001 1 2017 2017