ClinVar Miner

Submissions for variant NM_000660.7(TGFB1):c.918C>T (p.Leu306=)

gnomAD frequency: 0.00065  dbSNP: rs72480429
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
Eurofins Ntd Llc (ga) RCV000179334 SCV000231566 uncertain significance not provided 2015-04-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000179334 SCV001016086 benign not provided 2025-02-02 criteria provided, single submitter clinical testing

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