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: rs121913399
rs121913399
10 0.724 0.200 3 41224612 missense variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs28931589
rs28931589
13 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016