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: rs104894228
rs104894228
26 0.662 0.500 11 534286 missense variant C/A,G,T snp 0.010 1.000 1 2018 2018
dbSNP: rs121434595
rs121434595
19 0.692 0.357 1 114716124 missense variant C/A,G,T snp 0.010 1.000 1 2018 2018
dbSNP: rs121913535
rs121913535
9 0.784 0.250 12 25245348 missense variant C/A,G,T snp 0.010 1.000 1 2018 2018