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: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma
0.860 1.000 6 2010 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.810 1.000 1 2009 2019
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.800 1.000 15 2008 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.800 1.000 15 2008 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.740 1.000 4 2010 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
0.740 1.000 4 2009 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.740 1.000 4 2010 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.730 0.750 3 2013 2019
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.720 1.000 2 2010 2016
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Malignant neoplasm of urinary bladder
0.710 0.667 1 2010 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.710 0.667 1 2010 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 1.000 15 2009 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 11 2009 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.090 1.000 9 2009 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 0.800 5 2014 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0158646
Disease: Cleft palate with cleft lip
Cleft palate with cleft lip
0.040 1.000 4 2013 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.040 1.000 4 2013 2016
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.030 1.000 3 2011 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Experimental Organism Basal Cell Carcinoma
0.030 1.000 3 2011 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 1.000 2 2014 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.020 0.500 2 2013 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Squamous cell carcinoma of esophagus
0.020 0.500 2 2013 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Squamous cell carcinoma of the head and neck
0.010 1.000 1 2010 2010
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2009 2009
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence
0.010 1.000 1 2014 2014