Source: ALL

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: rs17581525
rs17581525
NFE2L2
2 177281634 intron variant C/G snv 0.26
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs35955110
rs35955110
NFE2L2
2 177278643 intron variant T/C snv 0.29
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs6433657
rs6433657
NFE2L2
2 177269949 intron variant A/G;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs2364725
rs2364725
NFE2L2
1.000 0.040 2 177268260 intron variant G/T snv 0.55
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2015 2015
dbSNP: rs4893819
rs4893819
NFE2L2
1.000 0.160 2 177266406 intron variant C/T snv 0.55
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		0.010 < 0.001 1 2019 2019
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.010 1.000 1 2016 2016
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2014 2014
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2019 2019
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 < 0.001 1 2016 2016
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 1.000 1 2016 2016
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2014 2014
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		0.010 1.000 1 2019 2019
dbSNP: rs35652124
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018