rs861539, KLC1;XRCC3

N. diseases: 60
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 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.800 2 1998 2000
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
1 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2010 2010
Malignant neoplasm of nasopharynx
CUI: C0153392
Disease: Malignant neoplasm of nasopharynx
1 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2010 2010
Metastatic Neoplasm
CUI: C2939420
Disease: Metastatic Neoplasm
4 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2018 2018
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
4 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1 2006 2006
Urothelial Carcinoma
CUI: C2145472
Disease: Urothelial Carcinoma
4 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2014 2014
Carcinoma, Transitional Cell
CUI: C0007138
Disease: Carcinoma, Transitional Cell
6 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2014 2014
Carcinoma breast stage IV
CUI: C0278488
Disease: Carcinoma breast stage IV
7 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2007 2007
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
9 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2015 2015
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
14 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1 2006 2006
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
23 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2014 2014
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
24 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2011 2011
Malignant neoplasm of large intestine
25 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2018 2018
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
26 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2005 2005
Experimental Organism Basal Cell Carcinoma
33 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2015 2015
Triple Negative Breast Neoplasms
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
37 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.020 1.000 2 2016 2016
Differentiated Thyroid Gland Carcinoma
37 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2016 2016
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
37 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2007 2007
Xeroderma Pigmentosum, Complementation Group D
39 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.070 1.000 7 2004 2015
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
40 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2009 2009
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
41 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.020 1.000 2 2005 2010
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
60 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.030 1.000 3 2007 2017
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
61 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.020 1.000 2 2005 2006
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
68 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2010 2010
Nijmegen Breakage Syndrome
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
72 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 0.010 1.000 1 2005 2005