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.
Paget Disease Extramammary
CUI: C0030186
Disease: Paget Disease Extramammary
1 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2012 2012
Acute dermatitis
CUI: C0262972
Disease: Acute dermatitis
2 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2013 2013
Genital Neoplasms, Female
CUI: C0017416
Disease: Genital Neoplasms, Female
4 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2017 2017
Malignant Female Reproductive System Neoplasm
5 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1 2017 2017
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
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
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
Myelofibrosis due to another disorder
6 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2018 2018
Urothelial Carcinoma
CUI: C2145472
Disease: Urothelial Carcinoma
10 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.020 1.000 2 2014 2015
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
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
Carcinoma, Transitional Cell
CUI: C0007138
Disease: Carcinoma, Transitional Cell
12 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.020 1.000 2 2014 2015
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
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2014 2014
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
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
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
17 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2009 2009
polyps
CUI: C0032584
Disease: polyps
18 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2011 2011
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
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
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.020 1.000 2 2012 2017
Adult Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2011 2011
Hepatitis A
CUI: C0019159
Disease: Hepatitis A
27 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2012 2012
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
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2011 2011