ClinVar Miner

Submissions for variant NM_004698.4(PRPF3):c.1203-10A>G

dbSNP: rs1337844716
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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 RCV001490308 SCV001694869 likely benign not provided 2019-09-14 criteria provided, single submitter clinical testing

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