ClinVar Miner

Submissions for variant NM_016169.4(SUFU):c.182+17G>T

dbSNP: rs2135599022
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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 RCV002095223 SCV002382198 likely benign Gorlin syndrome; Medulloblastoma 2022-04-24 criteria provided, single submitter clinical testing

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