rs10976993 PTPRD CXCL11 association
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Key takeaways
- This variant is linked to higher CXCL11 levels with a reported effect size of 4.65 p=3e-6 in about 318 people
- The association is based on a genome-wide association study catalog entry
- No rare disease effects are known for this common variant
Key takeaways
- This variant is linked to higher CXCL11 levels with a reported effect size of 4.65 p=3e-6 in about 318 people
- The association is based on a genome-wide association study catalog entry
- No rare disease effects are known for this common variant
What the research says This variant rs10976993 at PTPRD is associated with higher CXCL11 levels reported effect size 4.65 p=3e-6 in about 318 individuals [PMID 38326779]. The study uses a genome-wide association catalog to link the SNP to this protein level.
Reported associations CXCL11 This variant is linked to higher CXCL11 levels with a reported effect size of 4.65 p=3e-6 in about 318 individuals [PMID 38326779].
Evidence quality The supplied studies do not report a direct trait association for this variant; the rsid appears via GWAS Catalog entry PMID 38326779.
No lifestyle considerations on file for this variant.
Frequently asked questions
What does rs10976993 mean?
rs10976993 is a single nucleotide change in the PTPRD gene that has been linked to higher CXCL11 levels.
Is this variant dangerous?
The study shows only a modest association with CXCL11 and no evidence of disease risk.
Can I test for this variant?
Yes it is listed in public databases like the GWAS Catalog but testing requires a DNA sample analysis.