ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.1158-10C>T

dbSNP: rs904045520
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000457832 SCV000557089 likely benign Gorlin syndrome; Medulloblastoma 2024-01-03 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV002481491 SCV002774747 uncertain significance not provided 2021-08-13 criteria provided, single submitter clinical testing

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