ClinVar Miner

Submissions for variant NM_007055.4(POLR3A):c.646-316C>T

gnomAD frequency: 0.03879  dbSNP: rs72642276
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001787663 SCV002031183 likely benign not provided 2021-06-06 criteria provided, single submitter clinical testing

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