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: rs11575892
rs11575892
1 1.000 0.080 16 67483152 intron variant G/A snv 2.4E-02 2.5E-02 0.010 < 0.001 1 2009 2009
dbSNP: rs5030980
rs5030980
4 0.925 0.120 16 67483042 missense variant C/T snv 3.2E-02 2.9E-02 0.010 < 0.001 1 2009 2009