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: rs149037075
rs149037075
ABO
3 9 133255469 3 prime UTR variant CTGT/- delins 0.15 0.700 1.000 1 2016 2016
dbSNP: rs187099314
rs187099314
ABO
1 9 133255354 3 prime UTR variant C/G;T snv 0.700 1.000 1 2019 2019
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 2018 2018