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: rs757158
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2017 2017
dbSNP: rs757158
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs757158
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs757158
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2013 2013
dbSNP: rs757158
rs757158
PON1
0.851 0.240 7 95326216 upstream gene variant C/T snv 0.58
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		0.010 1.000 1 2013 2013
dbSNP: rs705382
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2015 2015
dbSNP: rs705382
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.010 1.000 1 2015 2015
dbSNP: rs705382
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2015 2015
dbSNP: rs705382
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs705382
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.010 1.000 1 2015 2015
dbSNP: rs854572
rs854572
PON1
7 95325384 upstream gene variant C/G snv 0.40
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		0.700 1.000 1 2012 2012
dbSNP: rs854571
rs854571
PON1
7 95325307 upstream gene variant T/C snv 0.62
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2013 2013
dbSNP: rs705381
rs705381
PON1
1.000 0.080 7 95324637 upstream gene variant T/C snv 0.72
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 < 0.001 1 2013 2013
dbSNP: rs705381
rs705381
PON1
1.000 0.080 7 95324637 upstream gene variant T/C snv 0.72
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 < 0.001 1 2013 2013
dbSNP: rs705379
rs705379
PON1
1.000 0.080 7 95324583 upstream gene variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2017 2017
dbSNP: rs705379
rs705379
PON1
1.000 0.080 7 95324583 upstream gene variant G/A;C;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3917481
rs3917481
PON1
1.000 0.040 7 95321453 intron variant C/T snv 3.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2015 2015
dbSNP: rs2237583
rs2237583
PON1
7 95320865 intron variant C/G;T snv
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		0.700 1.000 1 2013 2013
dbSNP: rs854566
rs854566
PON1
0.925 0.080 7 95319437 intron variant A/G snv 0.78
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity 		0.010 1.000 1 2013 2013
dbSNP: rs854566
rs854566
PON1
0.925 0.080 7 95319437 intron variant A/G snv 0.78
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2013 2013
dbSNP: rs2074351
rs2074351
PON1
1.000 0.080 7 95318487 non coding transcript exon variant G/A snv 0.26
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.010 1.000 1 2008 2008
dbSNP: rs765657236
rs765657236
PON1
1.000 0.120 7 95318360 synonymous variant G/A snv 8.0E-06
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.020 1.000 2 2016 2018
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 1.000 12 2000 2019
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.100 0.909 11 2002 2017
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.080 1.000 8 2002 2017