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: rs767932573
rs767932573
3 16 307299 intron variant G/A snv 5.0E-04 0.700 1.000 1 2017 2017
dbSNP: rs781191470
rs781191470
4 16 307744 intron variant G/A snv 3.1E-04 0.700 1.000 1 2016 2016