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: rs10509906
rs10509906
2 0.925 0.080 10 109997916 intron variant G/A;C snv 0.020 0.500 2 2014 2018
dbSNP: rs17095355
rs17095355
2 0.925 0.080 10 109975992 intron variant C/T snv 0.22 0.840 1.000 5 2010 2018