ClinVar Miner

Submissions for variant NM_000137.4(FAH):c.846G>A (p.Arg282=)

dbSNP: rs886334563
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002177846 SCV002350158 likely benign Tyrosinemia type I 2023-06-22 criteria provided, single submitter clinical testing

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