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: rs12814443
rs12814443
1 12 113479480 intron variant G/A snv 9.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs3809169
rs3809169
1 12 113473727 intron variant T/C snv 9.1E-02 0.700 1.000 1 2018 2018