rs2186037
This is a intron variant variant in the RSPO3 gene.
▶GWAS Catalog Trait Associations (35)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (35)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
cholesterol in very large VLDL measurement
total lipids in VLDL measurement
concentration of small VLDL particles
cholesteryl ester measurement
total lipids in small VLDL
cholesteryl esters in large VLDL measurement
cholesterol in very large HDL measurement
phospholipids in VLDL measurement
triglycerides to phosphoglycerides ratio
total lipids in very large HDL measurement
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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