ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.66C>A (p.Ala22=)

dbSNP: rs1265496966
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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 RCV001415898 SCV001618067 likely benign Gorlin syndrome; Medulloblastoma 2019-07-11 criteria provided, single submitter clinical testing

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