ClinVar Miner

Submissions for variant NM_012418.4(FSCN2):c.984-7C>T

gnomAD frequency: 0.00071  dbSNP: rs139335460
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000153281 SCV000202757 benign not specified 2014-03-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000904420 SCV001048935 likely benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000904420 SCV005214759 likely benign not provided criteria provided, single submitter not provided

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