rs2228001, XPC

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.
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1 2014 2014
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1 2014 2014
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2005 2005
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2013 2013
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2015 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2015 2015
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1 2019 2019
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1 2005 2005
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2010 2010
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2014 2014
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2010 2010
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.090 1.000 9 2005 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2010 2010
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.100 1.000 11 2005 2016
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.100 1.000 11 2005 2016
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2008 2008
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2013 2013
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2008 2008
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2015 2015
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.040 0.750 4 2007 2014
melanoma
CUI: C0025202
Disease: melanoma
515 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2014 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2010 2010
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.010 1.000 1 2014 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 0.070 1.000 7 2005 2019