ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.5900C>T (p.Ser1967Phe)

gnomAD frequency: 0.00001  dbSNP: rs1557176208
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
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529831 SCV001743986 uncertain significance not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001529831 SCV001808068 uncertain significance not provided no assertion criteria provided clinical testing

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