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: rs7849191
rs7849191
3 0.882 0.120 9 4988761 intron variant C/T snv 0.50 0.700 1.000 1 2008 2008
dbSNP: rs1159782
rs1159782
1 1.000 0.040 9 5078117 intron variant T/C snv 0.23 0.010 1.000 1 2018 2018
dbSNP: rs12343867
rs12343867
9 0.790 0.200 9 5074189 intron variant T/C snv 0.25 0.010 1.000 1 2018 2018