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Vitamin D levels

near SULT2A1 · rs117471111

What each result means

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

Questions about rs117471111

What is rs117471111?

rs117471111 is a single position in the genome, in or near the near SULT2A1 gene. Published research associates it with vitamin d levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs117471111 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 rs117471111 come from?

GWAS Catalog, Nat Genet 2021, PMID:33462484. 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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