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: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.030 1.000 3 2011 2019
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.010 1.000 1 2015 2015
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.030 0.667 3 2011 2019
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2011 2011
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		0.010 1.000 1 2018 2018
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.020 1.000 2 2013 2015
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma 		0.010 1.000 1 2010 2010
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma 		0.010 1.000 1 2010 2010
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma 		0.010 1.000 1 2006 2006
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.030 0.667 3 2004 2013
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.030 0.667 3 2004 2013
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: rs771025483
rs771025483
PON1
1.000 0.040 7 95306310 missense variant G/C snv 4.0E-06
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2010 2010
dbSNP: rs781071878
rs781071878
PON1
1.000 0.040 7 95311484 missense variant T/C snv 4.2E-04 1.0E-04
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2010 2010
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		0.010 1.000 1 2018 2018
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3 		0.010 1.000 1 2003 2003
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.010 1.000 1 2003 2003
dbSNP: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.090 0.667 9 2003 2014
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.050 0.800 5 2008 2012
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: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.030 1.000 3 2008 2019
dbSNP: rs854560
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.020 1.000 2 2009 2015
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: rs662
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome 		0.010 1.000 1 2004 2004
dbSNP: rs755603793
rs755603793
PON1
0.925 0.080 7 95308077 missense variant C/T snv 1.6E-05
CUI: C0002963
Disease: Angina Pectoris, Variant
Angina Pectoris, Variant 		0.010 1.000 1 2005 2005