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: rs516246
rs516246
10 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.800 1.000 1 2011 2011
dbSNP: rs601338
rs601338
19 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 0.700 1.000 1 2011 2011