ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.6154C>T (p.Leu2052=)

gnomAD frequency: 0.00003  dbSNP: rs372726521
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000287465 SCV000337789 uncertain significance not provided 2015-11-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000287465 SCV001067303 likely benign not provided 2024-03-08 criteria provided, single submitter clinical testing

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