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: rs121913412
rs121913412
19 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 0
dbSNP: rs137854578
rs137854578
APC
1 1.000 0.040 5 112839777 missense variant A/T snv 0.700 0
dbSNP: rs28931588
rs28931588
17 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 0
dbSNP: rs28931589
rs28931589
17 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 0
dbSNP: rs28934573
rs28934573
28 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs1042522
rs1042522
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2019 2019
dbSNP: rs11655237
rs11655237
17 0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 0.010 1.000 1 2019 2019
dbSNP: rs121913400
rs121913400
26 0.683 0.360 3 41224610 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs121913409
rs121913409
21 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs137854573
rs137854573
APC
10 0.807 0.120 5 112828889 stop gained C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs137854574
rs137854574
APC
4 0.925 0.120 5 112828919 stop gained C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs1389001294
rs1389001294
1 1.000 0.040 3 50331640 missense variant C/T snv 1.4E-05 0.010 1.000 1 2010 2010
dbSNP: rs202128953
rs202128953
1 1.000 0.040 11 20364346 stop gained G/A;T snv 7.2E-05 0.010 1.000 1 2010 2010
dbSNP: rs28933386
rs28933386
15 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs28934571
rs28934571
31 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2006 2006
dbSNP: rs4647924
rs4647924
49 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 0.010 1.000 1 2010 2010
dbSNP: rs762471803
rs762471803
6 0.925 0.040 11 102114201 missense variant T/G snv 0.010 1.000 1 2019 2019
dbSNP: rs763708092
rs763708092
1 1.000 0.040 1 204549443 missense variant G/A snv 8.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs768298443
rs768298443
2 1.000 0.040 10 112950932 missense variant C/A snv 4.1E-06 0.010 1.000 1 2019 2019
dbSNP: rs780571021
rs780571021
2 1.000 0.040 10 113146069 missense variant G/C;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs781124288
rs781124288
1 1.000 0.040 4 168139494 missense variant A/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs983496580
rs983496580
1 1.000 0.040 1 204526387 missense variant A/G snv 0.010 1.000 1 2010 2010