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: rs1057520030
rs1057520030
MET
7 116777427 missense variant A/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.700 1.000 1 2002 2002
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: rs369999291
rs369999291
APC
5 112767315 missense variant G/A snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs6842
rs6842
7 16794973 missense variant A/G;T snv 0.43 0.38
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2009 2009
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: rs863224683
rs863224683
17 7675224 missense variant G/A;C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs876659156
rs876659156
APC
5 112839714 missense variant G/A snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2004 2004
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: 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: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.100 1.000 21 2003 2019
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.030 1.000 3 2010 2015
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2014 2014
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: 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: 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: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
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: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2006 2006
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: rs5443
rs5443
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs2736100
rs2736100
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2016 2016
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: rs121434568
rs121434568
0.568 0.560 7 55191822 missense variant T/A;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2014 2015