ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.25405-34T>C

gnomAD frequency: 0.25362  dbSNP: rs16830090
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244213 SCV000307334 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001542971 SCV001761406 benign Arthrogryposis multiplex congenita 6 2021-07-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001542972 SCV001761407 benign Nemaline myopathy 2 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709450 SCV005245906 benign not provided criteria provided, single submitter not provided

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