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: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.790 0.900 9 2009 2018
dbSNP: rs1800625
rs1800625
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.720 0.667 2 2015 2019
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.990 98 2002 2020
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.989 95 2002 2020
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.933 45 2002 2019
dbSNP: rs1217691063
rs1217691063
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.976 41 2002 2019
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 39 2002 2019
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 39 2002 2019
dbSNP: rs2910164
rs2910164
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.941 34 2010 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 24 2002 2018
dbSNP: rs11614913
rs11614913
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.957 23 2011 2019
dbSNP: rs3746444
rs3746444
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.913 23 2011 2019
dbSNP: rs1052133
rs1052133
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.955 22 2002 2018
dbSNP: rs121434569
rs121434569
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 20 2007 2020
dbSNP: rs121912664
rs121912664
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.941 17 2005 2018
dbSNP: rs1463038513
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.824 17 1998 2016
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: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.824 17 1998 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.813 16 2003 2018
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 16 2008 2018
dbSNP: rs920778
rs920778
0.633 0.480 12 53966448 intron variant G/A snv 0.57
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.938 16 2015 2020
dbSNP: rs28934576
rs28934576
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.923 13 1993 2019
dbSNP: rs4938723
rs4938723
0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.846 13 2014 2019
dbSNP: rs77375493
rs77375493
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 13 2006 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.846 13 2004 2019
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.917 12 2002 2019