Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs876658923
rs876658923
1.000 0.120 3 36993593 frameshift variant TGAACCG/- delins
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs876659156
rs876659156
APC
5 112839714 missense variant G/A snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2004 2004
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs917411291
rs917411291
0.851 0.360 19 544072 start lost A/C;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 < 0.001 1 2009 2009
dbSNP: rs917570055
rs917570055
0.882 0.360 19 547342 start lost A/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 < 0.001 1 2009 2009
dbSNP: rs1217691063
rs1217691063
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs758272654
rs758272654
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2007 2010
dbSNP: rs121912651
rs121912651
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs1418016570
rs1418016570
6 161973326 missense variant G/C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1245554802
rs1245554802
0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs786202567
rs786202567
1.000 0.120 7 5992027 missense variant T/A;C snv 4.0E-06 1.4E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 < 0.001 1 2009 2009
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.100 1.000 23 2003 2019
dbSNP: rs577715207
rs577715207
0.827 0.160 3 189886413 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs231775
rs231775
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs763351020
rs763351020
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs767606327
rs767606327
4 99613118 missense variant T/C;G snv 1.2E-05; 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs587779333
rs587779333
0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 < 0.001 1 2009 2009
dbSNP: rs1801278
rs1801278
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs121913529
rs121913529
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs78311289
rs78311289
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.710 1.000 3 1999 2001
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2011 2018
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2008 2018
dbSNP: rs121913483
rs121913483
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.740 1.000 5 1999 2005