ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.3163G>A (p.Val1055Met)

dbSNP: rs9813235
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246057 SCV000307904 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000835392 SCV000977183 likely benign not provided 2020-06-30 criteria provided, single submitter clinical testing
Invitae RCV000835392 SCV001027777 likely benign not provided 2024-01-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000835392 SCV002050280 likely benign not provided 2021-10-08 criteria provided, single submitter clinical testing

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