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: rs74315316
rs74315316
4 0.925 0.080 1 34784797 missense variant G/A snv 0.010 1.000 1 2009 2009
dbSNP: rs74315317
rs74315317
3 1.000 0.080 1 34785018 missense variant T/A;C snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs74315321
rs74315321
5 0.882 0.080 1 34784887 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2009 2009