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: rs1333037
rs1333037
2 0.925 0.040 9 22040766 intron variant C/T snv 0.71 0.700 1.000 1 2016 2016
dbSNP: rs2041895
rs2041895
1 1.000 0.040 12 106956310 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs284491
rs284491
1 0.925 0.040 8 104946405 intron variant C/T snv 0.45 0.700 1.000 1 2016 2016