ClinVar Miner

Submissions for variant NM_001037333.3(CYFIP2):c.294C>T (p.Cys98=)

gnomAD frequency: 0.00003  dbSNP: rs368093712
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 RCV002015110 SCV002283083 benign not provided 2024-01-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002015110 SCV005188715 uncertain significance not provided criteria provided, single submitter not provided

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