ClinVar Miner

Submissions for variant NM_000137.4(FAH):c.645G>C (p.Pro215=)

dbSNP: rs151221329
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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 RCV001398665 SCV001600439 likely benign Tyrosinemia type I 2022-09-27 criteria provided, single submitter clinical testing

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