ClinVar Miner

Submissions for variant NM_001627.4(ALCAM):c.1524C>T (p.His508=)

gnomAD frequency: 0.00565  dbSNP: rs75636202
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000952889 SCV001099427 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000952889 SCV005093695 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing ALCAM: BP4, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000952889 SCV005300615 benign not provided criteria provided, single submitter not provided

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