ClinVar Miner

Submissions for variant NM_001312909.2(FAM111A):c.281_290del (p.Leu94fs)

dbSNP: rs759624749
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV002074044 SCV002010691 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074044 SCV002415017 benign not provided 2023-12-11 criteria provided, single submitter clinical testing

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