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.
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6
1 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.800 0
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
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2012 2012
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2007 2007
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2010 2010
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
CUI: C0007097
Disease: Carcinoma
103 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2006 2006
Carcinoma breast stage IV
CUI: C0278488
Disease: Carcinoma breast stage IV
14 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2006 2006
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
Childhood Acute Lymphoblastic Leukemia
261 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2018 2018
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2012 2012
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1 2005 2005
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
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2011 2011
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2016 2016
Deglutition Disorders
CUI: C0011168
Disease: Deglutition Disorders
50 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2009 2009
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2010 2010
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
Fibroid Tumor
CUI: C0023267
Disease: Fibroid Tumor
14 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2015 2015
Hematochezia
CUI: C0018932
Disease: Hematochezia
12 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2008 2008
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
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2018 2018
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
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2012 2012
Malignant neoplasm of nasopharynx
CUI: C0153392
Disease: Malignant neoplasm of nasopharynx
10 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2010 2010