ClinVar Miner

Submissions for variant NM_032228.6(FAR1):c.1176A>G (p.Glu392=)

gnomAD frequency: 0.01004  dbSNP: rs34341612
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001574381 SCV001801192 likely benign not provided 2020-05-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001574381 SCV002401320 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001574381 SCV005221345 likely benign not provided criteria provided, single submitter not provided

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