Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11292716
rs11292716
PON1
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269

2017
dbSNP: rs1157745
rs1157745
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs2057681
rs2057681
PON1
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		G 0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178

2013
dbSNP: rs2057681
rs2057681
PON1
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		G 0.700 GeneticVariation GWASDB Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk. 22982463

2012
dbSNP: rs2237583
rs2237583
PON1
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		0.700 GeneticVariation GWASDB Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL. 23160181

2013
dbSNP: rs3917502
rs3917502
PON1
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs3917510
rs3917510
PON1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs3917532
rs3917532
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs3917539
rs3917539
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		TAA 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs3917545
rs3917545
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs3917549
rs3917549
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs662
rs662
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs662
rs662
PON1
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO 		C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs662
rs662
PON1
CUI: C3149706
Disease: CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO 		C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs662
rs662
PON1
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs705379
rs705379
PON1
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
dbSNP: rs757158
rs757158
PON1
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		T 0.700 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269

2017
dbSNP: rs854560
rs854560
PON1
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs854560
rs854560
PON1
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO 		T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs854560
rs854560
PON1
CUI: C2674665
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding) 		T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs854572
rs854572
PON1
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		C 0.700 GeneticVariation GWASDB Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk. 22982463

2012