ClinVar Miner

Submissions for variant NM_001447.3(FAT2):c.6149G>A (p.Arg2050Gln)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003095334 SCV003484727 benign not provided 2023-10-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003095334 SCV004157463 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing FAT2: BP4, BS2

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