ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.84462C>T (p.Pro28154=)

dbSNP: rs1703705150
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001391891 SCV001593523 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-10-13 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005237776 SCV005886132 likely benign not specified 2025-02-10 criteria provided, single submitter clinical testing

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