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: rs497309
rs497309
5 0.882 0.240 6 31924707 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4151667
rs4151667
9 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 0.010 1.000 1 2014 2014