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Left ventricular mass (indexed to body surface area)

CMIP · rs72831120

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−8, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 36,083 European or unknown ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.407 lower (95% confidence interval 0.26-0.55); p = 3 × 10−8.

How common The A allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 16, band 16q23.3 — in an intron of CMIP.

What each result means

A/A Two copies of the version the research linked to Left ventricular mass (indexed to body surface area). 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 Left ventricular mass (indexed to body surface area). That is a smaller link than two copies.
G/G No copy of the version the research linked to Left ventricular mass (indexed to body surface area). This is the starting point the study compared everyone against.
Source
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros R, Zheng SL, Grace C, Jordà P, Francis C, West DM, Jurgens SJ, Thomson KL, Harper AR, Ormondroyd E, Xu X, Theotokis PI
and 50 more — show all
Buchan RJ, McGurk KA, Mazzarotto F, Boschi B, Pelo E, Lee M, Noseda M, Varnava A, Vermeer AMC, Walsh R, Amin AS, van Slegtenhorst MA, Roslin NM, Strug LJ, Salvi E, Lanzani C, de Marvao A, Roberts JD, Tremblay-Gravel M, Giraldeau G, Cadrin-Tourigny J, L'Allier PL, Garceau P, Talajic M, Gagliano Taliun SA, Pinto YM, Rakowski H, Pantazis A, Bai W, Baksi J, Halliday BP, Prasad SK, Barton PJR, O'Regan DP, Cook SA, de Boer RA, Christiaans I, Michels M, Kramer CM, Ho CY, Neubauer S, Matthews PM, Wilde AAM, Tardif JC, Olivotto I, Adler A, Goel A, Ware JS, Bezzina CR, Watkins H
Hypergenes InterOmics Collaborators · HCMR Investigators
Nature genetics · 2025 · PMID 39966646 · open access

Questions about rs72831120

What is rs72831120?

rs72831120 is a single position in the genome, in or near the CMIP gene. Published research associates it with left ventricular mass (indexed to body surface area). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs72831120 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 rs72831120 come from?

GWAS Catalog, Nature genetics 2025, PMID:39966646. 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.

Left ventricular mass (indexed to body surface area) (rs72831120). MyGeneLog™. https://www.mygenelog.com/variants/rs72831120

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