Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.030 1.000 3 2011 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.030 1.000 3 2011 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.030 0.667 3 2014 2017
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.030 1.000 3 2011 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2014 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.020 1.000 2 2015 2019
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2014 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 2014 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		0.020 1.000 2 2015 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0.020 1.000 2 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		0.020 1.000 2 2015 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.020 1.000 2 2015 2015
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2012 2012
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C4722099
Disease: High grade glioma
High grade glioma 		0.010 1.000 1 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		0.010 1.000 1 2018 2018
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma 		0.010 1.000 1 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		0.010 1.000 1 2018 2018
dbSNP: rs2298881
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2016 2016