ClinVar Miner

Submissions for variant NM_173500.4(TTBK2):c.603+17G>C

gnomAD frequency: 0.01219  dbSNP: rs115190236
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002254089 SCV002525329 likely benign not provided 2021-12-03 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV002254089 SCV003034068 benign not provided 2025-01-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002254089 SCV005214558 likely benign not provided criteria provided, single submitter not provided

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