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: rs150840924
rs150840924
7 0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs3131917
rs3131917
3 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 0.010 1.000 1 2018 2018
dbSNP: rs35677470
rs35677470
6 0.807 0.160 3 58197909 missense variant G/A;C snv 4.8E-02; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs6314
rs6314
23 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 0.010 1.000 1 2008 2008
dbSNP: rs7574685
rs7574685
2 0.925 0.040 2 234702877 intron variant T/C snv 0.59 0.010 1.000 1 2017 2017