ClinVar Miner

Submissions for variant NM_000428.3(LTBP2):c.4905G>C (p.Leu1635=)

gnomAD frequency: 0.00137  dbSNP: rs144520047
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241859 SCV000304205 likely benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000241859 SCV000342030 benign not specified 2016-06-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000913256 SCV001058399 benign not provided 2025-01-28 criteria provided, single submitter clinical testing

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