ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.8223_8224delinsTC (p.Lys2742Gln)

dbSNP: rs886038896
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000246209 SCV000318881 uncertain significance Cardiovascular phenotype 2013-08-07 criteria provided, single submitter clinical testing There is insufficient or conflicting evidence for classification of this alteration.

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