ClinVar Miner

Submissions for variant NM_012301.4(MAGI2):c.2616C>T (p.Asn872=)

gnomAD frequency: 0.00051  dbSNP: rs148005928
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000296073 SCV000336727 likely benign not specified 2015-11-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059149 SCV002393485 benign not provided 2025-01-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494840 SCV002798620 likely benign Nephrotic syndrome 15 2021-11-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002059149 SCV005220426 likely benign not provided criteria provided, single submitter not provided

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