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: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 0.909 33 2005 2019
dbSNP: rs1458511470
rs1458511470
2 201272639 frameshift variant -/C delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs17524488
rs17524488
0.925 0.040 4 87975555 non coding transcript exon variant -/G delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs11267092
rs11267092
F2R
5 76715788 intron variant -/GGCCGCGGGAAGC;GGCCGCGGGAAGCGGCCGCGGGAAGC delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs10680577
rs10680577
0.776 0.160 19 40798690 intron variant -/TACT delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs866419664
rs866419664
0.882 0.040 17 7673821 frameshift variant -/TCCCA delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs3830675
rs3830675
1.000 0.040 10 87931195 intron variant -/TCTTA delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2014 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs17880560
rs17880560
17 7668169 intron variant -/TGGCCG delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs71305152
rs71305152
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs397509239
rs397509239
1.000 17 43057122 frameshift variant A/- del
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs144848
rs144848
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.060 1.000 6 2002 2017
dbSNP: rs61764370
rs61764370
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 0.750 4 2011 2017
dbSNP: rs712
rs712
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 1.000 4 2015 2019
dbSNP: rs1566734
rs1566734
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 0.333 3 2008 2019
dbSNP: rs1042667
rs1042667
1.000 0.040 17 72124410 3 prime UTR variant A/C snv 0.41 0.36
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs1056628
rs1056628
20 46016407 3 prime UTR variant A/C snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs1057519697
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs1190488467
rs1190488467
4 86701433 missense variant A/C snv 8.1E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2010 2010
dbSNP: rs1204382931
rs1204382931
0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs16892766
rs16892766
0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs2072671
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs2239704
rs2239704
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs2296972
rs2296972
0.925 0.080 13 46854336 intron variant A/C snv 0.70
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2017 2017
dbSNP: rs2410373
rs2410373
0.851 0.120 8 16066997 intergenic variant A/C snv 0.34
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2007 2007