ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.1711G>A (p.Val571Met)

dbSNP: rs760127618
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001964873 SCV002197912 likely benign not provided 2022-09-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001964873 SCV003832756 uncertain significance not provided 2019-11-15 criteria provided, single submitter clinical testing

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