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: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.080 1.000 8 2008 2016
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.050 1.000 5 2008 2016
dbSNP: rs121912664
rs121912664
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.050 1.000 5 2005 2018
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.050 1.000 5 2008 2016
dbSNP: rs28934576
rs28934576
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.040 1.000 4 2005 2018
dbSNP: rs762846821
rs762846821
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.040 1.000 4 2012 2015
dbSNP: rs11540652
rs11540652
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 1.000 2 2015 2018
dbSNP: rs1057519747
rs1057519747
0.716 0.280 17 7675094 missense variant A/C;G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2008 2008
dbSNP: rs1131691021
rs1131691021
0.716 0.120 17 7675097 missense variant A/C;G snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2015 2015
dbSNP: rs121912651
rs121912651
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2007 2007
dbSNP: rs121912660
rs121912660
0.683 0.240 17 7673781 missense variant C/A;G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2019 2019
dbSNP: rs121912665
rs121912665
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2008 2008
dbSNP: rs28934575
rs28934575
0.641 0.400 17 7674230 missense variant C/A;G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2018 2018
dbSNP: rs573154688
rs573154688
1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2018 2018
dbSNP: rs730882025
rs730882025
0.724 0.360 17 7674885 missense variant C/A;G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013
dbSNP: rs764803020
rs764803020
0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2019 2019
dbSNP: rs771939956
rs771939956
17 7670705 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2018 2018
dbSNP: rs779196500
rs779196500
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017
dbSNP: rs781490101
rs781490101
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2019 2019
dbSNP: rs863224682
rs863224682
1.000 0.080 17 7669655 missense variant C/A;T snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs863224683
rs863224683
17 7675224 missense variant G/A;C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013
dbSNP: rs879253942
rs879253942
0.677 0.400 17 7673826 missense variant A/G snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs942158624
rs942158624
0.724 0.320 17 7674948 missense variant T/A snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017