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: rs1052717
rs1052717
3 0.925 0.080 22 41885425 intron variant A/G snv 0.62 0.010 1.000 1 2008 2008
dbSNP: rs2267439
rs2267439
3 1.000 0.080 22 41841765 intron variant C/G;T snv 0.010 1.000 1 2008 2008
dbSNP: rs2267443
rs2267443
5 0.882 0.120 22 41891450 intron variant A/G snv 0.67 0.010 1.000 1 2008 2008