ClinVar Miner

Submissions for variant NM_006486.3(FBLN1):c.279G>T (p.Thr93=)

dbSNP: rs765918593
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177258 SCV000229101 uncertain significance not provided 2015-03-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000177258 SCV001067955 likely benign not provided 2022-05-25 criteria provided, single submitter clinical testing

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