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: rs104894361
rs104894361
5 0.846 0.214 12 25245370 missense variant T/A,C,G snp 4.0E-06 0.700 1 2003 2003
dbSNP: rs112445441
rs112445441
17 0.699 0.286 12 25245347 missense variant snp 0.700 0
dbSNP: rs121908382
rs121908382
3 0.923 0.071 1 45331530 missense variant G/A snp 0.700 2 2004 2016
dbSNP: rs121908383
rs121908383
3 0.923 0.071 1 45331502 missense variant T/C snp 0.700 2 2004 2016
dbSNP: rs121909776
rs121909776
3 0.923 0.071 2 201187798 missense variant T/C snp 1.2E-04 9.6E-05 0.700 1 2002 2002
dbSNP: rs121912469
rs121912469
3 0.923 0.071 5 132489457 missense variant T/A snp 0.700 1 1998 1998
dbSNP: rs121912470
rs121912470
3 0.878 0.107 5 132489448 missense variant A/G snp 0.700 1 1999 1999
dbSNP: rs121913528
rs121913528
4 0.878 0.071 12 25227349 missense variant C/A,T snp 0.700 2 1992 2003
dbSNP: rs121913529
rs121913529
70 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 0.700 8 1984 2015
dbSNP: rs121913530
rs121913530
39 0.615 0.321 12 25245351 missense variant C/A,G,T snp 0.700 0
dbSNP: rs28933369
rs28933369
5 0.878 0.071 17 39724744 missense variant G/A snp 0.700 2 2004 2007
dbSNP: rs28933379
rs28933379
APC
3 0.923 0.071 5 112838953 missense variant G/A snp 0.700 0
dbSNP: rs372481703
rs372481703
APC
2 0.923 0.071 5 112839106 missense variant G/A snp 1.6E-05 3.2E-05 0.700 0
dbSNP: rs4986791
rs4986791
108 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 0.010 1.000 1 2009 2009