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: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.020 1.000 2 2013 2013
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.020 1.000 2 2013 2013
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.020 1.000 2 2013 2013
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		0.010 1.000 1 2015 2015
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C3274515
Disease: Severe Bronchopulmonary Dysplasia
Severe Bronchopulmonary Dysplasia 		0.010 1.000 1 2015 2015
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2018 2018
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		0.010 < 0.001 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.010 1.000 1 2018 2018
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
Childhood Renal Cell Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2015 2015
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2018 2018
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2020 2020
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2020 2020
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		0.010 < 0.001 1 2016 2016
dbSNP: rs6721961
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2016 2016