rs2116942

This variant is located in the S1PR2 gene.

GWAS Catalog Trait Associations (5)

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

neutrophil count

Allele G
OR
p 5.0e-25
N 627,215
Large GWAS
multi-ancestry

alkaline phosphatase measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.02
p 1.0e-16
N 463,178
Large GWAS
multi-ancestry

systolic blood pressure

Allele T
OR 0.22
p 7.0e-10
N 459,777
Large GWAS
multi-ancestry

reticulocyte amount

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.01
p 5.0e-9
N 408,112
Large GWAS
European

reticulocyte count

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.02
p 3.0e-10
N 408,112
Large GWAS
European

ClinVar annotation

Likely Benign★★★
3 submitters3 publications

not provided; S1PR2-related disorder

View on ClinVar →

About S1PR2

This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]

View all S1PR2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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