Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10885997
rs10885997
Entrez Id: 5408
Gene Symbol: PNLIPRP2
PNLIPRP2
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs10885997
rs10885997
Entrez Id: 5408
Gene Symbol: PNLIPRP2
PNLIPRP2
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs7910135
rs7910135
Entrez Id: 5408
Gene Symbol: PNLIPRP2
PNLIPRP2
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs10885997
rs10885997
Entrez Id: 5408
Gene Symbol: PNLIPRP2
PNLIPRP2
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		G 0.700 GeneticVariation GWASCAT Exome-wide association study of plasma lipids in >300,000 individuals. 29083408 2017
dbSNP: rs4751995
rs4751995
Entrez Id: 5408
Gene Symbol: PNLIPRP2
PNLIPRP2
CUI: C0149521
Disease:
Pancreatitis, Chronic 		0.010 GeneticVariation BEFREE Here, we tested the hypothesis that variant p.W358X might increase risk for chronic pancreatitis through acinar cell stress. 30408063 2018