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: rs863225349
rs863225349
APC
2 1.000 0.120 5 112839531 missense variant A/G snv 0.700 0
dbSNP: rs869312784
rs869312784
APC
1 5 112838674 missense variant A/G snv 0.700 0
dbSNP: rs2229080
rs2229080
DCC
16 0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 0.010 1.000 1 1997 1997
dbSNP: rs1801166
rs1801166
APC
17 0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 0.010 1.000 1 1998 1998
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2002 2002
dbSNP: rs370662884
rs370662884
3 0.925 0.080 3 41225816 synonymous variant G/A snv 3.2E-05 4.9E-05 0.010 1.000 1 2003 2003
dbSNP: rs1463038513
rs1463038513
APC
36 0.658 0.440 5 112839511 frameshift variant TAAA/- delins 0.030 1.000 3 1998 2005
dbSNP: rs1801155
rs1801155
APC
42 0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 0.030 1.000 3 1998 2005
dbSNP: rs587780424
rs587780424
1 3 12433975 missense variant A/C snv 0.010 1.000 1 2005 2005
dbSNP: rs1057519739
rs1057519739
2 1.000 0.080 18 51065518 missense variant G/A;C snv 0.700 1.000 7 1996 2007
dbSNP: rs1057519740
rs1057519740
1 18 51065532 missense variant C/A snv 0.700 1.000 7 1996 2007
dbSNP: rs1057519741
rs1057519741
1 18 51078417 missense variant G/T snv 0.700 1.000 7 1996 2007
dbSNP: rs281875324
rs281875324
3 1.000 0.120 18 51065456 missense variant A/C;G snv 0.700 1.000 7 1996 2007
dbSNP: rs10808555
rs10808555
6 0.925 0.080 8 127397266 intron variant G/A snv 0.65 0.010 1.000 1 2008 2008
dbSNP: rs1222213359
rs1222213359
62 0.574 0.720 6 43770966 missense variant G/A snv 0.010 < 0.001 1 2008 2008
dbSNP: rs138551214
rs138551214
4 0.925 0.080 1 22909025 missense variant G/A snv 4.0E-06 1.4E-05 0.700 1.000 1 2008 2008
dbSNP: rs1566734
rs1566734
10 0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 0.010 1.000 1 2008 2008
dbSNP: rs7837328
rs7837328
8 0.882 0.120 8 127410882 intron variant A/G snv 0.52 0.010 1.000 1 2008 2008
dbSNP: rs9929218
rs9929218
16 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.700 1.000 1 2008 2008
dbSNP: rs10936599
rs10936599
32 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 0.700 1.000 1 2010 2010
dbSNP: rs11169552
rs11169552
10 0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs4925386
rs4925386
14 0.776 0.080 20 62345988 intron variant T/C snv 0.56 0.700 1.000 1 2010 2010
dbSNP: rs6691170
rs6691170
12 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs719725
rs719725
7 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 0.010 1.000 1 2010 2010
dbSNP: rs1057519725
rs1057519725
6 0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 0.700 1.000 8 2005 2011