ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.978A>T (p.Pro326=)

dbSNP: rs2135888873
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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 RCV001476988 SCV001681210 likely benign Gorlin syndrome; Medulloblastoma 2019-02-06 criteria provided, single submitter clinical testing

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