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: rs1033313160
rs1033313160
9 125506375 missense variant G/T snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2017 2017
dbSNP: rs104894403
rs104894403
0.851 0.240 13 20189386 missense variant C/A;G;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2006 2006
dbSNP: rs3918242
rs3918242
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2017 2017
dbSNP: rs531564
rs531564
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2018 2018
dbSNP: rs774390402
rs774390402
16 75235116 missense variant A/C snv 1.2E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2008 2008
dbSNP: rs8179090
rs8179090
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 < 0.001 1 2017 2017
dbSNP: rs121434569
rs121434569
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 0.500 2 2013 2016
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.100 0.927 41 2007 2018
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.100 0.927 41 2007 2018
dbSNP: rs121913500
rs121913500
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.050 1.000 5 2014 2020
dbSNP: rs28934578
rs28934578
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.040 1.000 4 2009 2018
dbSNP: rs28934576
rs28934576
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.030 1.000 3 2007 2017
dbSNP: rs751295137
rs751295137
0.851 0.160 7 55152582 missense variant G/A snv 8.0E-06 7.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.030 1.000 3 2009 2015
dbSNP: rs760101437
rs760101437
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.030 1.000 3 2009 2015
dbSNP: rs1049074086
rs1049074086
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2007 2012
dbSNP: rs1057519847
rs1057519847
0.570 0.560 7 55191821 missense variant CT/AG mnv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2015 2018
dbSNP: rs1057519848
rs1057519848
0.570 0.560 7 55191822 missense variant TG/GT mnv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2015 2018
dbSNP: rs121434568
rs121434568
0.568 0.560 7 55191822 missense variant T/A;G snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2015 2018
dbSNP: rs121909218
rs121909218
0.672 0.360 10 87933145 missense variant G/A snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2002 2004
dbSNP: rs121913529
rs121913529
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2012 2017
dbSNP: rs121917887
rs121917887
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2003 2007
dbSNP: rs1418810723
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2007 2011
dbSNP: rs2070600
rs2070600
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.020 1.000 2 2008 2014
dbSNP: rs1022088103
rs1022088103
16 55485759 missense variant G/A snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2007 2007
dbSNP: rs1046282
rs1046282
0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2019 2019