Standard

Height

ABCB1 · rs2032588

Where this position leads

Condition: Height

rs2032588 Condition: Height Height Condition rs2032588 rs2032588 ABCB1

What the study found

Who was studied 5,314,291 European ancestry, Hispanic or Latin American, East Asian ancestry, African ancestry, South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0197 higher (95% confidence interval 0.017-0.022); p = 1 × 10−51.

How common The A allele had a frequency of about 6% in the people studied.

Where it sits Chromosome 7, band 7q21.12 — in an intron of ABCB1.

What ClinVar records

Classification drug response for Tramadol response; no assertion criteria provided (0 of 4 stars, 1 submitter), last evaluated 2018-04-28. ClinVar record 829475 NM_001348946.2(ABCB1):c.1350+44C>T

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

A/A 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.
A/G One copy of the version the research linked to Height. That is a smaller link than two copies.
G/G No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
Source

Questions about rs2032588

What is rs2032588?

rs2032588 is a single position in the genome, in or near the ABCB1 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 rs2032588 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.

Does having rs2032588 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 rs2032588 come from?

GWAS Catalog, Nature 2022, PMID:36224396. 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 (rs2032588). MyGeneLog™. https://www.mygenelog.com/variants/rs2032588

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