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: rs104894228
rs104894228
0.605 0.560 11 534286 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2014 2014
dbSNP: rs1057519816
rs1057519816
0.763 0.200 17 39711955 missense variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2012 2014
dbSNP: rs1057519824
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2003 2007
dbSNP: rs1057519837
rs1057519837
1.000 0.040 3 41224631 missense variant C/G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2011 2014
dbSNP: rs1057519855
rs1057519855
0.776 0.120 11 533873 missense variant CT/AC;TC mnv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2014 2014
dbSNP: rs121913246
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2007 2017
dbSNP: rs121913343
rs121913343
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2014 2014
dbSNP: rs121913496
rs121913496
0.724 0.440 11 533873 missense variant C/A;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2010 2014
dbSNP: rs28933369
rs28933369
0.925 0.080 17 39724744 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.710 1.000 1 2011 2014
dbSNP: rs1003129577
rs1003129577
3 39094706 missense variant G/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs10053538
rs10053538
0.807 0.160 5 157110499 intron variant C/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs10069690
rs10069690
0.595 0.560 5 1279675 intron variant C/T snv 0.36
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs10074991
rs10074991
0.851 0.120 5 40790449 intron variant G/A snv 0.31
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs1007541
rs1007541
0.882 0.080 2 48981895 intron variant C/T snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs10079250
rs10079250
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs10090154
rs10090154
0.807 0.160 8 127519892 intergenic variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs1010898370
rs1010898370
1.000 2 208243469 missense variant T/C;G snv 8.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs1011329790
rs1011329790
0.925 0.080 7 30504681 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2018 2018
dbSNP: rs1012477
rs1012477
0.827 0.160 1 7798075 intron variant G/C snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs1014509103
rs1014509103
1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs10165970
rs10165970
0.708 0.320 2 100840527 intron variant G/A snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs1017621656
rs1017621656
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2001 2001
dbSNP: rs10204525
rs10204525
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1020833107
rs1020833107
9 132398145 synonymous variant G/A snv 7.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2017 2017
dbSNP: rs10235235
rs10235235
0.925 0.080 7 99478208 intron variant T/C snv 0.13
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 < 0.001 1 2014 2014