Standard

Body mass index

ADCY6 · rs3730071

Where this position leads

Conditions: Childhood Body Mass Index, Obesity and Body Weight

rs3730071 Condition: Childhood Body Mass Index Childhood Body Mass Index Condition Condition: Obesity and Body Weight Obesity and Body Weight Condition rs3730071 rs3730071 ADCY6

What the study found

Who was studied 1,122,049 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0284 higher (95% confidence interval 0.021-0.036); p = 2 × 10−12.

Where it sits Chromosome 12, band 12q13.12 — a missense change in ADCY6.

What ClinVar records

Classification Benign for ADCY6-related disorder; no assertion criteria provided (0 of 4 stars, 1 submitter), last evaluated 2019-07-11. ClinVar record 3055951 NM_015270.5(ADCY6):c.2020G>T (p.Ala674Ser)

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 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 No copy of the version the research linked to Body mass index. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Body mass index. That is a smaller link than two copies.
C/C Two copies of the version the research linked to Body mass index. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs3730071

What is rs3730071?

rs3730071 is a single position in the genome, in or near the ADCY6 gene. Published research associates it with body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3730071 linked to?

On MyGeneLog this position is linked to Childhood Body Mass Index, Obesity and Body Weight. The research behind each link, and its sources, are set out on that condition page.

Does having rs3730071 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 rs3730071 come from?

GWAS Catalog, Nature communications 2022, PMID:36581621. 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.

Body mass index (rs3730071). MyGeneLog™. https://www.mygenelog.com/variants/rs3730071

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