Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56873913
rs56873913
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs56873913
rs56873913
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. 31268507 2019
dbSNP: rs56873913
rs56873913
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256 2017
dbSNP: rs111544199
rs111544199
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs552708909
rs552708909
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0018935
Disease:
Hematocrit procedure 		CT 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs56873913
rs56873913
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs56873913
rs56873913
Entrez Id: 5639;51070
Gene Symbol: PRRG2;NOSIP
PRRG2;NOSIP
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Biological insights from 108 schizophrenia-associated genetic loci. 25056061 2014