ClinVar Miner

Submissions for variant NM_020702.5(MYORG):c.1245C>G (p.Pro415=)

dbSNP: rs1185459546
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002238906 SCV002509113 likely benign not provided 2022-12-02 criteria provided, single submitter clinical testing

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