ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.1026G>T (p.Val342=)

dbSNP: rs1232642116
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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 RCV000934347 SCV001080068 likely benign Majeed syndrome 2022-06-21 criteria provided, single submitter clinical testing

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