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: rs1805015
rs1805015
22 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 0.010 1.000 1 2008 2008
dbSNP: rs1805016
rs1805016
3 0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 0.010 1.000 1 2008 2008