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Height

CYP19A1 · rs3751599

Where this position leads

Condition: Height

rs3751599 Condition: Height Height Condition rs3751599 rs3751599 CYP19A1

What the study found

Who was studied 6,534 Han Chinese ancestry individuals; replicated in 1,881 Han Chinese ancestry individuals from 637 families.

The effect Each copy of the G allele shifted the measure 0.187 higher (95% confidence interval 0.13-0.25); p = 5 × 10−10.

How common The G allele had a frequency of about 93% in the people studied.

Where it sits Chromosome 15, band 15q21.2 — in an intron of MIR4713HG.

What each result means

A/A No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Height. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs3751599

What is rs3751599?

rs3751599 is a single position in the genome, in or near the CYP19A1 gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3751599 linked to?

On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs3751599?

Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs3751599 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 rs3751599 come from?

GWAS Catalog, Hum Genet 2013, PMID:23456168. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Height (rs3751599). MyGeneLog™. https://www.mygenelog.com/variants/rs3751599

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