ClinVar Miner

Submissions for variant NM_001040167.2(LFNG):c.672C>T (p.Tyr224=)

gnomAD frequency: 0.00012  dbSNP: rs151012354
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251003 SCV000306222 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001429628 SCV001632345 likely benign Spondylocostal dysostosis 3, autosomal recessive 2024-01-25 criteria provided, single submitter clinical testing

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