ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.1864+12C>T

gnomAD frequency: 0.00287  dbSNP: rs78381731
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001512014 SCV001719351 benign not provided 2024-01-26 criteria provided, single submitter clinical testing
GeneDx RCV001512014 SCV001768567 likely benign not provided 2020-01-22 criteria provided, single submitter clinical testing

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