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: rs16850871
rs16850871
1 1 230083723 intron variant A/G snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs7513659
rs7513659
1 1 230090639 intron variant G/A snv 8.5E-02 0.700 1.000 1 2018 2018