Source: BEFREE

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: rs10036748
rs10036748
0.752 0.360 5 151078585 intron variant C/A;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2016 2016
dbSNP: rs1018379423
rs1018379423
1 22907986 missense variant G/T snv 4.0E-06 2.1E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2012 2012
dbSNP: rs10254120
rs10254120
0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs1042028
rs1042028
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs1045485
rs1045485
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2006 2006
dbSNP: rs1047840
rs1047840
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2012 2012
dbSNP: rs1048638
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2012 2012
dbSNP: rs104893859
rs104893859
0.925 0.080 4 110618669 missense variant C/G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2011 2011
dbSNP: rs1051740
rs1051740
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2011 2011
dbSNP: rs1051992
rs1051992
11 6319476 missense variant A/G snv 4.2E-06; 0.55 0.51
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2012 2012
dbSNP: rs1056836
rs1056836
0.581 0.680 2 38071060 missense variant G/C snv 0.51
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
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: 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: rs1057519865
rs1057519865
0.742 0.240 3 138946321 missense variant G/C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017
dbSNP: rs1057519903
rs1057519903
0.683 0.080 1 226064434 missense variant A/T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017
dbSNP: rs1057519921
rs1057519921
0.763 0.240 2 177234231 missense variant T/C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2011 2011
dbSNP: rs1057520009
rs1057520009
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017
dbSNP: rs11134527
rs11134527
0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013
dbSNP: rs11214077
rs11214077
0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2015 2015
dbSNP: rs112295309
rs112295309
1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2017 2017
dbSNP: rs11283943
rs11283943
MCC
0.882 0.160 5 113071088 splice donor variant -/CGCACTGTCTTCCT;CGCGCTGTCTTCCT;CGTGCTGTCTTCCT delins
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2011 2011
dbSNP: rs1130409
rs1130409
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
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: rs113561019
rs113561019
1.000 0.080 3 9756791 missense variant G/A;T snv 3.9E-03; 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013