Standard

Dilated cardiomyopathy 1G

TTN · rs876658077

Where this position leads

Strength of the evidence

There is no record yet to score this position by (a ClinVar disease classification or a genome-wide significant study). That is not the same as weak evidence.

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 ClinVar records

Classification Uncertain significance; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 3 submitters), last evaluated 2025-03-18. ClinVar record 229498 NM_001267550.2(TTN):c.68498C>T (p.Ser22833Leu)

Classification Pathogenic/Likely pathogenic for Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2025-02-20. ClinVar record 379497 NM_001267550.2(TTN):c.68498C>G (p.Ser22833Ter)

Change history MyGeneLog™ keeps a copy of every weekly release from 2026-10-19 and compares them. This position's classification has not changed since.

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 ClinVar lists as disease-causing or likely disease-causing for Dilated cardiomyopathy 1G. A result like this should be confirmed by a medical genetic test and talked through with a doctor; consumer DNA files can misread rare variants. (ClinVar VCV000379497, criteria provided, multiple submitters, no conflicts)

C/G One copy of the version ClinVar lists as disease-causing or likely disease-causing for Dilated cardiomyopathy 1G. Some conditions need only one copy; for others, one copy makes a person a carrier who is usually healthy but can pass it on. A genetic counsellor can say which applies. (ClinVar VCV000379497, criteria provided, multiple submitters, no conflicts)

G/G No copy of the version ClinVar lists as disease-causing or likely disease-causing for Dilated cardiomyopathy 1G. This is the usual result. (ClinVar VCV000379497, criteria provided, multiple submitters, no conflicts)

Source: ClinVar VCV000379497, criteria provided, multiple submitters, no conflicts

Questions about rs876658077

What is rs876658077?

rs876658077 is a single position in the genome, in or near the TTN gene. Published research associates it with dilated cardiomyopathy 1g. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs876658077 linked to?

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

Does having rs876658077 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 rs876658077 come from?

ClinVar VCV000379497, criteria provided, multiple submitters, no conflicts. 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.

Dilated cardiomyopathy 1G (rs876658077). MyGeneLog™. https://www.mygenelog.com/variants/rs876658077

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