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: rs73243607
rs73243607
1 4 23757039 intron variant C/T snv 3.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs7667050
rs7667050
1 4 23811486 intron variant T/A;C snv 0.700 1.000 1 2019 2019