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
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
5 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1 2005 2005
Oral Submucous Fibrosis
CUI: C0029172
Disease: Oral Submucous Fibrosis
8 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
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
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
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
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
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
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
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
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
19 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2016 2016
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
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
Primary differentiated carcinoma of thyroid gland
41 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2016 2016
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
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
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2007 2011
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.030 1.000 3 2014 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
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2011 2011
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
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
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2015 2016
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