rs1936807

This is a intron variant variant in the RSPO3 gene.

GWAS Catalog Trait Associations (6)

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

hemoglobin measurement

Allele C
OR
β 0.022
p 7.0e-24
N 684,122
Large GWAS
European
Allele C
OR 0.02
p 5.0e-12
N 172,925
Large GWAS
European

cholesteryl esters to total lipids in small LDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele G
OR 0.03
p 1.0e-20
N 241,027
Large GWAS
European

triglyceride measurement, physical activity

Allele C
OR
p 2.0e-12
N 102,281
Large GWAS
multi-ancestry

lymphocyte 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 6.0e-12
N 408,112
Large GWAS
European

erythrocyte count

Allele G
OR 0.02
p 5.0e-11
N 172,952
Large GWAS
European

BMI-adjusted waist circumference

Allele G
OR 0.03
p 2.0e-10
N 122,328
Meta-analysisLarge GWAS
multi-ancestry

About RSPO3

This gene belongs to the R-spondin family. The encoded protein plays a role in the regulation of Wnt (wingless-type MMTV integration site family)/beta-catenin and Wnt/planar cell polarity (PCP) signaling pathways, which are involved in development, cell growth and disease pathogenesis. Genome-wide association studies suggest a correlation of this gene with bone mineral density and risk of fracture. This gene may be involved in tumor development. [provided by RefSeq, Jul 2013]

View all RSPO3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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