ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.435A>G (p.Thr145=)

dbSNP: rs867742294
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001452398 SCV001656060 likely benign Majeed syndrome 2022-07-26 criteria provided, single submitter clinical testing

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