ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.621+9G>T

dbSNP: rs1360878639
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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 RCV001452675 SCV001656347 likely benign not provided 2019-10-13 criteria provided, single submitter clinical testing

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