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: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.030 1.000 3 2009 2016
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.030 1.000 3 2009 2016
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs1057519903
rs1057519903
0.683 0.080 1 226064434 missense variant A/T snv
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2016 2016
dbSNP: rs10889677
rs10889677
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs121913243
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 1998 1998
dbSNP: rs121913500
rs121913500
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs121918464
rs121918464
0.708 0.440 12 112450406 missense variant G/A;C snv
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2011 2011
dbSNP: rs1284110310
rs1284110310
0.882 0.200 17 39706999 missense variant G/A snv 7.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs1374154597
rs1374154597
1.000 0.120 3 136023097 frameshift variant -/G delins
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs372032595
rs372032595
DLD
0.925 0.080 7 107904960 missense variant T/G snv 4.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2016 2016
dbSNP: rs4245739
rs4245739
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs55819519
rs55819519
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs562015640
rs562015640
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2011 2011
dbSNP: rs746354996
rs746354996
15 66489734 missense variant G/A snv 2.8E-05 7.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2019 2019
dbSNP: rs762846821
rs762846821
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs777980327
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2016 2016
dbSNP: rs799917
rs799917
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013
dbSNP: rs878854066
rs878854066
0.439 0.800 17 7676153 missense variant GG/AC mnv
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 1.000 1 2013 2013