rs1799782, XRCC1

N. diseases: 151
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.920 25 2001 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.917 24 2001 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
995 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.818 22 2001 2015
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1000 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.818 22 2001 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.818 22 2001 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.917 12 2002 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.917 12 2002 2019
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
320 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.030 1.000 3 2002 2009
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.030 1.000 3 2003 2005
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
24 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2003 2003
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
171 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.060 0.833 6 2004 2018
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.030 0.667 3 2004 2011
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
12 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2004 2004
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 1.000 10 2005 2016
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 1.000 10 2005 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.050 0.800 5 2005 2017
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
167 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2005 2005
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2005 2005
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
102 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2005 2005
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2005 2005
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
5 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2005 2005
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
24 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2005 2005
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
238 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.060 0.833 6 2006 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
236 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.060 0.833 6 2006 2019
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
94 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.060 1.000 6 2006 2011