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: rs1805193
rs1805193
1 1.000 0.040 1 169733631 5 prime UTR variant C/A snv 8.3E-02 7.8E-02 0.010 1.000 1 2013 2013
dbSNP: rs5361
rs5361
47 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2013 2013