Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11219769
rs11219769
Entrez Id: 23584
Gene Symbol: VSIG2
VSIG2
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs11604175
rs11604175
Entrez Id: 23584
Gene Symbol: VSIG2
VSIG2
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: rs12541
rs12541
Entrez Id: 23584;90952
Gene Symbol: VSIG2;ESAM
VSIG2;ESAM
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE Two schizophrenia-associated NRGN SNPs (rs12807809 and rs12541) were tested for association with working memory-elicited dorsolateral prefrontal cortex (DLPFC) activity and surface-wide cortical thickness. 24098564 2013
dbSNP: rs2075713
rs2075713
Entrez Id: 23584
Gene Symbol: VSIG2
VSIG2
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE We did not detect any evidence of association of schizophrenia with any SNPs; however, two nominal associations of rs12278912 (OR = 1.10, P = 0.057) and rs2075713 (OR = 1.10, P = 0.057) were observed. 22461181 2012