ClinVar Miner

Submissions for variant NM_001386140.1(MTTP):c.1233C>T (p.Leu411=)

dbSNP: rs1179169124
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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 RCV001441897 SCV001644837 likely benign not provided 2023-09-21 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578627 SCV001805881 likely benign Abetalipoproteinaemia 2021-07-14 criteria provided, single submitter clinical testing

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