ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1157+14C>T

dbSNP: rs2063675828
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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 RCV002165997 SCV002425510 likely benign Gorlin syndrome; Medulloblastoma 2022-01-12 criteria provided, single submitter clinical testing

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