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: rs1057519853
rs1057519853
0.851 0.080 9 77794572 missense variant TG/AA mnv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2018 2018
dbSNP: rs121913492
rs121913492
0.790 0.160 9 77794572 missense variant T/A;C;G snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2018 2018
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2008 2008
dbSNP: rs12826786
rs12826786
0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2017 2017
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2010 2010
dbSNP: rs13428812
rs13428812
0.827 0.120 2 25269598 intron variant A/G snv 0.31
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2019 2019
dbSNP: rs149617956
rs149617956
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2016 2016
dbSNP: rs1799983
rs1799983
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2019 2019
dbSNP: rs1801516
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2016 2016
dbSNP: rs201894482
rs201894482
5 138557977 missense variant G/A snv 6.0E-05 2.1E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2015 2015
dbSNP: rs2070744
rs2070744
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2019 2019
dbSNP: rs3732379
rs3732379
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2005 2005
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2008 2008
dbSNP: rs751478142
rs751478142
1.000 5 138570994 missense variant G/A snv 2.8E-05 1.4E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2015 2015
dbSNP: rs760583024
rs760583024
1.000 0.080 11 18934156 missense variant G/A;T snv 8.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2018 2018
dbSNP: rs765189442
rs765189442
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2011 2011
dbSNP: rs775514340
rs775514340
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2011 2011
dbSNP: rs920778
rs920778
0.633 0.480 12 53966448 intron variant G/A snv 0.57
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 < 0.001 1 2015 2015
dbSNP: rs1057519912
rs1057519912
0.776 0.200 X 71129408 missense variant C/G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2013 2016
dbSNP: rs11547328
rs11547328
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2002 2003
dbSNP: rs17822931
rs17822931
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2011 2019
dbSNP: rs2297518
rs2297518
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2010 2017
dbSNP: rs3746444
rs3746444
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2011 2015
dbSNP: rs771138120
rs771138120
0.827 0.120 9 21971191 missense variant G/A;C;T snv 9.1E-06; 4.5E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 0.500 2 2002 2003
dbSNP: rs1057519847
rs1057519847
0.570 0.560 7 55191821 missense variant CT/AG mnv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.030 0.667 3 2012 2016