ClinVar Miner

Submissions for variant NM_002476.2(MYL4):c.100_102dup (p.Pro34dup)

gnomAD frequency: 0.00001  dbSNP: rs759787679
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001209798 SCV001381248 uncertain significance Atrial fibrillation, familial, 18 2023-10-28 criteria provided, single submitter clinical testing This variant, c.100_102dup, results in the insertion of 1 amino acid(s) of the MYL4 protein (p.Pro34dup), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs759787679, gnomAD 0.005%). This variant has not been reported in the literature in individuals affected with MYL4-related conditions. ClinVar contains an entry for this variant (Variation ID: 940256). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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