Standard

IgA nephropathy

CFHR3 · rs6677604

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of IgA nephropathy — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with IgA nephropathy.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of IgA nephropathy compared to the general population.
Source

Questions about rs6677604

What is rs6677604?

rs6677604 is a single position in the genome, in or near the CFHR3 gene. Published research associates it with iga nephropathy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6677604 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs6677604 come from?

GWAS Catalog, Nat Genet 2014, PMID:25305756. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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