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: rs9686661
rs9686661
3 1.000 0.080 5 56565959 intron variant C/T snv 0.20 0.800 1.000 4 2010 2018
dbSNP: rs11743303
rs11743303
2 5 56564125 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs154254
rs154254
1 5 56524757 intron variant G/C snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs459193
rs459193
9 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs465002
rs465002
3 5 56512648 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs9687833
rs9687833
3 1.000 0.080 5 56565774 intron variant G/A snv 0.21 0.700 1.000 1 2018 2018