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
CUI: C3151417
Disease: 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
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: 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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.889 27 2003 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.889 27 2003 2019
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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.636 22 2004 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.636 22 2004 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.636 22 2004 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.933 15 2004 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 1.000 13 2004 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.846 13 2004 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.100 0.846 13 2004 2019
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.080 0.750 8 2004 2015
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
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
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
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
CUI: C2752147
Disease: 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
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
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
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2007 2016
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