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: rs651007
rs651007 		22 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 0.800 1.000 2 2010 2017
dbSNP: rs579459
rs579459 		28 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 1 2009 2009
dbSNP: rs11220471
rs11220471
ST3GAL4
1 11 126396770 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs2519093
rs2519093
ABO
16 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs507666
rs507666
ABO
8 1.000 0.040 9 133273983 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs8176720
rs8176720
ABO
3 9 133257486 synonymous variant T/A;C;G snv 0.40 0.40 0.700 1.000 1 2017 2017