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: rs59893503
rs59893503
1 7 47397677 intron variant G/A snv 2.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs865603
rs865603
1 7 47417868 intron variant C/A;G snv 0.700 1.000 1 2016 2016