ClinVar Miner

Submissions for variant NM_006486.3(FBLN1):c.185+4C>T

gnomAD frequency: 0.00296  dbSNP: rs147045275
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 RCV000969753 SCV001117284 benign not provided 2024-12-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000969753 SCV005274245 benign not provided criteria provided, single submitter not provided

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