Genopathy
Gene-Disorder Association · Article
Gene
TNNC1
Troponin C1, Slow Skeletal And Cardiac Type
Disorder
Atrial Fibrillation, Familial, 12
First reported 1997
Key publication · disorder Identification of a genetic locus for familial atrial fibrillation.The New England journal of medicine · 1997
Manually curated
Association Review

In brief

The association between TNNC1 (Troponin C1, Slow Skeletal And Cardiac Type) and Atrial Fibrillation, Familial, 12 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 4
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
TNNC1

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Atrial Fibrillation, Familial, 12

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

1 clinical feature

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Provenance

References & sources

4 references

Every source and publication cited across this dossier, as one numbered reference list.

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