ClinVar Miner

Submissions for variant NM_145261.4(DNAJC19):c.56-17G>C

dbSNP: rs2473933857
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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 RCV003599884 SCV004460601 likely benign 3-methylglutaconic aciduria type 5 2023-04-17 criteria provided, single submitter clinical testing

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