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: rs121908566
rs121908566
1 1.000 0.120 7 92040690 missense variant C/T snv 8.2E-06 0.700 1.000 1 2007 2007
dbSNP: rs730880043
rs730880043
1 1.000 0.120 7 92001406 stop gained G/T snv 0.700 0