rs28379706

This is a protein-altering variant in the PLXNB2 gene.

GWAS Catalog Trait Associations (6)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

plexin-B2 measurement

Allele C
OR 1.21
p 6.0e-103
N 466
Small GWAS
African American or Afro-Caribbean

blood protein amount

Allele C
OR 0.39
p 8.0e-102
N 5,365
Large GWAS
European

r-spondin-2 measurement

Allele C
OR 1.19
p 8.0e-55
N 196
Small GWAS
European

hypertension

Allele T
OR 5.90
p 4.0e-9
N 1,317,884
Meta-analysisLarge GWAS
multi-ancestry

pulse pressure measurement

Allele T
OR 0.09
p 4.0e-8
N 1,164,961
Meta-analysisLarge GWAS
European

systolic blood pressure

Allele T
OR 0.14
p 5.0e-8
N 810,865
Meta-analysisLarge GWAS
European

About PLXNB2

Members of the B class of plexins, such as PLXNB2 are transmembrane receptors that participate in axon guidance and cell migration in response to semaphorins (Perrot et al. (2002) [PubMed 12183458]).[supplied by OMIM, Mar 2008]

View all PLXNB2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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