ClinVar Miner

Submissions for variant NM_000137.4(FAH):c.961-5T>C

dbSNP: rs2142107684
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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 RCV002139302 SCV002465956 likely benign Tyrosinemia type I 2021-04-10 criteria provided, single submitter clinical testing

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