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: rs1801155
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.020 1.000 2 2003 2005
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: rs1049074086
rs1049074086
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1057519736
rs1057519736
0.752 0.160 15 90088605 missense variant C/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1057519855
rs1057519855
0.776 0.120 11 533873 missense variant CT/AC;TC mnv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1057519883
rs1057519883
0.742 0.280 9 21971120 missense variant C/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs1057520039
rs1057520039
0.882 0.200 19 1207169 stop gained C/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs1060503115
rs1060503115
0.763 0.400 7 5978664 missense variant T/A;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2011 2011
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: rs11615
rs11615
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs121434265
rs121434265
0.925 0.080 1 193125142 stop gained C/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
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: 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: 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: rs121912664
rs121912664
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs121913233
rs121913233
0.627 0.520 11 533874 missense variant T/A;C;G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs121913273
rs121913273
0.605 0.440 3 179218294 missense variant G/A;C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs121913400
rs121913400
0.683 0.360 3 41224610 missense variant C/A;G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2001 2001
dbSNP: rs121913403
rs121913403
0.683 0.240 3 41224622 missense variant C/A;G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 1998 1998
dbSNP: rs121913412
rs121913412
0.724 0.280 3 41224633 missense variant A/C;G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 1998 1998
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: 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: rs1258159645
rs1258159645
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06
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: rs1383461329
rs1383461329
1.000 0.120 12 123389469 missense variant C/T snv 1.4E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2019 2019