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: rs62636503
rs62636503
3 0.882 0.080 8 24953779 missense variant C/T snv 0.800 1.000 4 2004 2016
dbSNP: rs58982919
rs58982919
10 0.790 0.080 8 24956223 missense variant T/C snv 0.800 1.000 4 2004 2016