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: rs13042395
rs13042395
13 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 0.040 0.750 4 2015 2019
dbSNP: rs3746803
rs3746803
2 1.000 0.080 20 763738 missense variant G/A;C snv 0.10; 1.2E-05 0.020 1.000 2 2011 2016
dbSNP: rs3746802
rs3746802
1 1.000 0.080 20 763664 missense variant T/C snv 0.10 9.3E-02 0.010 1.000 1 2011 2011
dbSNP: rs3746804
rs3746804
1 1.000 0.080 20 763771 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2014 2014