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: rs121909602
rs121909602
1 1.000 0.080 19 35651302 missense variant G/A snv 1.6E-05 0.800 1.000 1 2008 2008
dbSNP: rs778740017
rs778740017
3 0.925 0.120 19 35651301 missense variant C/T snv 4.0E-06 0.700 0