ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1144-10C>T

dbSNP: rs1159181079
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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 RCV001454026 SCV001657736 likely benign Fanconi anemia 2020-02-18 criteria provided, single submitter clinical testing

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