ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.9363T>G (p.Pro3121=)

dbSNP: rs6709886
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000667241 SCV000791661 likely benign Nemaline myopathy 2 2017-05-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000667241 SCV001015864 likely benign Nemaline myopathy 2 2024-01-21 criteria provided, single submitter clinical testing

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