rs6721961, NFE2L2

N. diseases: 24
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.020 1.000 2 2013 2013
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.020 1.000 2 2013 2013
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.020 1.000 2 2013 2013
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2012 2012
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2015 2015
Childhood Renal Cell Carcinoma
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
10 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2020 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2020 2020
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2016 2016
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2018 2018
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2012 2012
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2018 2018
Necrotizing enterocolitis in fetus OR newborn
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
26 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2018 2018
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2019 2019
Severe Bronchopulmonary Dysplasia
CUI: C3274515
Disease: Severe Bronchopulmonary Dysplasia
2 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 0.010 1.000 1 2015 2015