ClinVar Miner

Submissions for variant NM_005573.4(LMNB1):c.360-19C>T

gnomAD frequency: 0.00844  dbSNP: rs74640805
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522968 SCV001732608 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501846 SCV002806457 likely benign Adult-onset autosomal dominant demyelinating leukodystrophy; Microcephaly 26, primary, autosomal dominant 2021-07-21 criteria provided, single submitter clinical testing

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