Standard

DNA methylation (parent-of-origin)

near SFRP2 · rs13135284

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of DNA methylation (parent-of-origin) compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with DNA methylation (parent-of-origin).
T/T Published research associates this genotype with typical/baseline likelihood of DNA methylation (parent-of-origin) — no copies of the reported risk allele.
Source

Questions about rs13135284

What is rs13135284?

rs13135284 is a single position in the genome, in or near the near SFRP2 gene. Published research associates it with dna methylation (parent-of-origin). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13135284 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 rs13135284 come from?

GWAS Catalog, Twin Res Hum Genet 2013, PMID:23725790. 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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