ClinVar Miner

Submissions for variant NM_000137.4(FAH):c.607-10C>T

dbSNP: rs2041245977
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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 RCV001479406 SCV001683701 likely benign Tyrosinemia type I 2021-08-26 criteria provided, single submitter clinical testing

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