PLXNB2, plexin B2, 23654

N. diseases: 19; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5771118
rs5771118
Entrez Id: 23654
Gene Symbol: PLXNB2
PLXNB2
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs28394672
rs28394672
Entrez Id: 23654
Gene Symbol: PLXNB2
PLXNB2
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs28573806
rs28573806
Entrez Id: 23654
Gene Symbol: PLXNB2
PLXNB2
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs28578714
rs28578714
Entrez Id: 23654
Gene Symbol: PLXNB2
PLXNB2
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs79966207
rs79966207
Entrez Id: 23654
Gene Symbol: PLXNB2
PLXNB2
CUI: C0018498
Disease:
Hair Color 		C 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018