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: rs73072483
rs73072483
2 3 50734193 intron variant G/A snv 9.6E-02 0.700 1.000 2 2016 2019
dbSNP: rs73078622
rs73078622
1 3 51333892 intron variant A/G snv 5.0E-02 0.700 1.000 1 2016 2016