ClinVar Miner

Submissions for variant NM_001375808.2(LPIN2):c.288+13G>C

dbSNP: rs2143137276
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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 RCV002204412 SCV002495514 likely benign Majeed syndrome 2021-06-05 criteria provided, single submitter clinical testing

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