ClinVar Miner

Submissions for variant NM_007055.4(POLR3A):c.885+19C>G

gnomAD frequency: 0.01064  dbSNP: rs12263414
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001512932 SCV001720433 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
GeneDx RCV001512932 SCV002027811 likely benign not provided 2021-05-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001512932 SCV005221754 likely benign not provided criteria provided, single submitter not provided

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