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
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
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
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2005 2005
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2005 2006
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
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
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
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
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
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
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
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2010 2010
Squamous cell carcinoma of the head and neck
348 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2002 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
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
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
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2012 2012
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
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
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
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
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2012 2012
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2012 2012