ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.911-8C>T

dbSNP: rs771361493
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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 RCV001477648 SCV001681894 likely benign Gorlin syndrome; Medulloblastoma 2024-01-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003311995 SCV004010013 uncertain significance not provided 2023-06-01 criteria provided, single submitter clinical testing SUFU: PM2:Supporting, BP4

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