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: rs112445441
rs112445441
32 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.700 0
dbSNP: rs1203145163
rs1203145163
1 1.000 0.080 21 42363329 missense variant C/A snv 7.0E-06 0.700 0
dbSNP: rs1400295986
rs1400295986
APC
2 0.925 0.080 5 112838233 missense variant T/C snv 0.700 0
dbSNP: rs1555515731
rs1555515731
4 0.882 0.160 16 68812189 frameshift variant T/- delins 0.700 0
dbSNP: rs180177133
rs180177133
9 0.807 0.240 16 23614089 frameshift variant T/- delins 1.2E-05 1.4E-05 0.700 0
dbSNP: rs202208566
rs202208566
1 1.000 0.080 12 109903156 missense variant T/C snv 6.5E-04 1.7E-04 0.700 0
dbSNP: rs367807476
rs367807476
1 1.000 0.080 19 1223035 missense variant C/G;T snv 9.2E-06 1.4E-05 0.700 0
dbSNP: rs372481703
rs372481703
APC
1 1.000 0.080 5 112839106 missense variant G/A snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs555607708
rs555607708
33 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 0.700 0
dbSNP: rs587780537
rs587780537
5 0.925 0.080 16 68810224 missense variant G/A snv 0.700 0
dbSNP: rs10719
rs10719
24 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 0.010 < 0.001 1 2017 2017
dbSNP: rs111238176
rs111238176
4 0.851 0.160 1 172665840 missense variant A/G snv 0.010 < 0.001 1 2013 2013
dbSNP: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 < 0.001 1 2015 2015
dbSNP: rs1135354
rs1135354
3 0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 0.010 < 0.001 1 2015 2015
dbSNP: rs1143627
rs1143627
47 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 0.010 < 0.001 1 2018 2018
dbSNP: rs11536878
rs11536878
5 0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 0.010 < 0.001 1 2014 2014
dbSNP: rs1165109290
rs1165109290
2 0.925 0.080 6 159692850 synonymous variant G/A snv 4.2E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs13361189
rs13361189
13 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 0.010 < 0.001 1 2012 2012
dbSNP: rs1353702185
rs1353702185
79 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 0.010 < 0.001 1 2014 2014
dbSNP: rs1447295
rs1447295
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 < 0.001 1 2017 2017
dbSNP: rs1457547311
rs1457547311
4 0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs1562430
rs1562430
6 0.807 0.160 8 127375606 intron variant T/C snv 0.41 0.010 < 0.001 1 2015 2015
dbSNP: rs16944
rs16944
92 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 0.010 < 0.001 1 2018 2018
dbSNP: rs174546
rs174546
17 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 0.010 < 0.001 1 2018 2018
dbSNP: rs174583
rs174583
16 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.010 < 0.001 1 2018 2018