ClinVar Miner

Submissions for variant NM_201550.4(LRRC10):c.768G>A (p.Ala256=)

gnomAD frequency: 0.00056  dbSNP: rs148566929
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000539489 SCV000659737 benign Dilated Cardiomyopathy, Dominant 2024-01-18 criteria provided, single submitter clinical testing
GeneDx RCV001755920 SCV002007789 likely benign not provided 2021-04-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001755920 SCV005216119 likely benign not provided criteria provided, single submitter not provided

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