ClinVar Miner

Submissions for variant NM_015425.6(POLR1A):c.1114C>A (p.Arg372=)

dbSNP: rs752860605
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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 RCV000895926 SCV001039993 likely benign not provided 2018-01-19 criteria provided, single submitter clinical testing

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