Standard

Diastolic blood pressure

TTN · rs56207956

Where this position leads

Condition: Blood Pressure

rs56207956 Condition: Blood Pressure Blood Pressure Condition rs56207956 rs56207956 TTN

What the study found

Who was studied 526,001 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.245 lower (95% confidence interval 0.17-0.32); p = 8 × 10−11.

Where it sits Chromosome 2, band 2q31.2 — a synonymous change in TTN.

What ClinVar records

Classification Benign/Likely benign for Cardiovascular phenotype, Tibial muscular dystrophy, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Early-onset myopathy with fatal cardiomyopathy and 2 more; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 18 submitters), last evaluated 2026-02-04. ClinVar record 47704 NM_001267550.2(TTN):c.106275G>C (p.Gly35425=)

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

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

Questions about rs56207956

What is rs56207956?

rs56207956 is a single position in the genome, in or near the TTN gene. Published research associates it with diastolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs56207956 linked to?

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

Does having rs56207956 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 rs56207956 come from?

GWAS Catalog, Investigative ophthalmology & visual science 2022, PMID:35762941. 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.

Diastolic blood pressure (rs56207956). MyGeneLog™. https://www.mygenelog.com/variants/rs56207956

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