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: rs587777162
rs587777162
5 0.925 0.040 20 63495972 missense variant C/T snv 0.700 1.000 2 2012 2013
dbSNP: rs1555883505
rs1555883505
10 0.827 0.160 20 63490712 missense variant G/A snv 0.700 1.000 1 2016 2016