rs1799782, XRCC1

N. diseases: 151
Source: ALL
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.
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2003 2003
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
13 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2004 2004
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
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 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
213 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
82 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2005 2005
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2006 2006
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2007 2007
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Hyperkeratosis
CUI: C0870082
Disease: Hyperkeratosis
19 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Keratosis
CUI: C0022593
Disease: Keratosis
10 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Melanosis
CUI: C0025209
Disease: Melanosis
23 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Melanosis coli
CUI: C0221391
Disease: Melanosis coli
5 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Salivary gland carcinoma
CUI: C0948750
Disease: Salivary gland carcinoma
5 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2007 2007
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2008 2008
TARSAL-CARPAL COALITION SYNDROME
CUI: C1861305
Disease: TARSAL-CARPAL COALITION SYNDROME
13 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2008 2008
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.030 1.000 3 2002 2009
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2009 2009
Breast Fibrocystic Disease
CUI: C0016034
Disease: Breast Fibrocystic Disease
12 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2009 2009