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: rs492488
rs492488
ABO
3 9 133269548 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs676996
rs676996
ABO
1 9 133270647 intron variant G/T snv 0.700 1.000 1 2019 2019