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: rs115025532
rs115025532
1 1.000 0.080 22 50032791 intron variant G/A;C snv 2.5E-02 0.700 1.000 1 2018 2018