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.
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
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.070 1.000 7 2008 2019
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2008 2019
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2008 2019
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2014 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
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 1.000 4 2008 2018
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 0.750 4 2015 2018
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 0.750 4 2015 2018
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.040 0.750 4 2015 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.030 1.000 3 2013 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.030 1.000 3 2013 2018
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 0.500 2 2009 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.020 1.000 2 2016 2018
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: 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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1.000 1 2018 2018
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 0.010 1 2018 2018