rs25489, XRCC1

N. diseases: 78
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.
Adult Myelodysplastic Syndrome
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
20 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2016 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2008 2008
Amyotrophic Lateral Sclerosis, Sporadic
90 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2010 2010
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.080 0.875 8 2007 2017
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2008 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.070 0.714 7 2003 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.080 0.875 8 2007 2017
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2016 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.100 0.900 10 2001 2019
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2017 2017
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2018 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.050 0.200 5 2012 2017
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.050 0.200 5 2012 2017
Childhood Acute Lymphoblastic Leukemia
261 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.030 1.000 3 2007 2012
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2013 2013
Childhood Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
20 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2016 2016
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2018 2018
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1 2018 2018
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1 2009 2009
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.040 1.000 4 2010 2013
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2015 2015
Differentiated Thyroid Gland Carcinoma
80 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.030 1.000 3 2013 2014
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2010 2010
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.010 1.000 1 2013 2013