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: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.920 25 2001 2018
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.917 24 2001 2018
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 0.818 22 2001 2015
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 0.818 22 2001 2015
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 0.818 22 2001 2015
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 0.917 12 2002 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
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
Squamous cell carcinoma of esophagus
0.030 1.000 3 2002 2009
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.030 1.000 3 2003 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
0.010 1.000 1 2003 2003
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
Squamous cell carcinoma of the head and neck
0.060 0.833 6 2004 2018
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0007114
Disease: Malignant neoplasm of skin
Malignant neoplasm of skin
0.030 0.667 3 2004 2011
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0.010 < 0.001 1 2004 2004
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 1.000 10 2005 2016
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.100 1.000 10 2005 2016
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.050 0.800 5 2005 2017
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
0.010 < 0.001 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0001430
Disease: Adenoma
Adenoma
0.010 1.000 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
0.010 1.000 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 1.000 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
0.010 1.000 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0850639
Disease: premalignant lesion
premalignant lesion
0.010 < 0.001 1 2005 2005
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.060 0.833 6 2006 2019
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
Xeroderma Pigmentosum, Complementation Group D
0.060 1.000 6 2006 2011
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.060 0.833 6 2006 2019