rs861539, KLC1;XRCC3

N. diseases: 104
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.
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2013 2013
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2013 2013
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2013 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.080 1.000 8 2009 2014
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.080 1.000 8 2009 2014
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.070 1.000 7 2009 2014
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.070 0.857 7 2003 2014
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2005 2014
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 0.750 4 2011 2014
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2005 2014
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2008 2014
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2006 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2013 2014
leukemia
CUI: C0023418
Disease: leukemia
144 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2014 2014
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2008 2014
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 0.500 2 2014 2014
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Carcinoma, Transitional Cell
CUI: C0007138
Disease: Carcinoma, Transitional Cell
12 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Urothelial Carcinoma
CUI: C2145472
Disease: Urothelial Carcinoma
10 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.080 0.750 8 2004 2015