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: rs1325394060
rs1325394060
9 0.851 0.320 X 53534144 missense variant C/G;T snv 9.5E-06 0.700 0
dbSNP: rs1556914274
rs1556914274
13 0.790 0.440 X 53537626 missense variant G/A snv 0.700 0
dbSNP: rs1557036757
rs1557036757
7 0.925 0.240 X 53647375 missense variant G/A snv 0.700 0
dbSNP: rs1557036768
rs1557036768
44 0.708 0.320 X 53647390 missense variant C/T snv 0.700 0