ClinVar Miner

Submissions for variant NM_000137.4(FAH):c.606+8A>G

dbSNP: rs1444983943
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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 RCV001393723 SCV001595397 likely benign Tyrosinemia type I 2024-02-06 criteria provided, single submitter clinical testing

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