Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2057681
rs2057681
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
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
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
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
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: rs854572
rs854572
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