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: rs3731239
rs3731239
10 0.763 0.240 9 21974219 intron variant A/G snv 0.26 0.020 1.000 2 2008 2014
dbSNP: rs3731249
rs3731249
23 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 0.020 1.000 2 2007 2009
dbSNP: rs1453633223
rs1453633223
6 0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs200863613
rs200863613
6 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 0.010 1.000 1 2017 2017
dbSNP: rs878853646
rs878853646
3 0.882 0.080 9 21971106 missense variant C/A;T snv 4.3E-06; 8.6E-06 0.010 1.000 1 2009 2009