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: rs121913237
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2015
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2006 2019
dbSNP: rs1250394819
rs1250394819
TMED7 ; TMED7-TICAM2 ; LOC101927100
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2017
dbSNP: rs1444669684
rs1444669684
CDKN2A ; CDKN2B-AS1
0.658 0.480 9 21994285 missense variant C/A;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2014 2016
dbSNP: rs1452231640
rs1452231640
POLB
1.000 0.080 8 42339015 missense variant T/C snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2019 2019
dbSNP: rs1463038513
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 1998 2007
dbSNP: rs1800449
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2016
dbSNP: rs1800566
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2017
dbSNP: rs1800625
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2015
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: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 1998 2007
dbSNP: rs1801166
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2003 2009
dbSNP: rs187084
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2012 2019
dbSNP: rs1979277
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2007 2014
dbSNP: rs281864719
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2014 2019
dbSNP: rs34301344
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2006 2006
dbSNP: rs4938723
rs4938723
BTG4 ; MIR34B ; MIR34C ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2016 2017
dbSNP: rs568887534
rs568887534
DCTN6
0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2015 2017
dbSNP: rs752021744
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2014 2015
dbSNP: rs755100942
rs755100942
ARL11
0.724 0.320 13 49630894 stop gained G/A snv 4.2E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2006 2006
dbSNP: rs777980327
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2010 2013
dbSNP: rs863225281
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2014 2019
dbSNP: rs876658657
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 1.000 2 2008 2011
dbSNP: rs10036748
rs10036748
TNIP1
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
EPHB2
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
PMS2
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