ClinVar Miner

Submissions for variant NM_001037333.3(CYFIP2):c.621G>A (p.Ser207=)

dbSNP: rs199855067
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 RCV002074830 SCV002430870 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002074830 SCV004157910 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing CYFIP2: BP4, BP7

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