ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.92682C>T (p.Phe30894=)

dbSNP: rs2154147790
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002214183 SCV002496572 uncertain significance not provided 2022-02-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005225564 SCV005866028 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-05-01 criteria provided, single submitter clinical testing

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