ClinVar Miner

Submissions for variant NM_006486.3(FBLN1):c.2025G>A (p.Lys675=)

gnomAD frequency: 0.00026  dbSNP: rs190890810
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083352 SCV002380871 benign not provided 2023-10-17 criteria provided, single submitter clinical testing

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