ClinVar Miner

Submissions for variant NM_032737.4(LMNB2):c.265-6C>T

gnomAD frequency: 0.00015  dbSNP: rs267607650
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001079325 SCV001063950 likely benign Progressive myoclonic epilepsy type 9; Lipodystrophy, partial, acquired, susceptibility to 2024-10-22 criteria provided, single submitter clinical testing
OMIM RCV000015560 SCV000035825 risk factor Acquired partial lipodystrophy 2006-08-01 no assertion criteria provided literature only
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057199 SCV000088312 not provided not provided no assertion provided not provided

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