ClinVar Miner

Submissions for variant NM_032737.4(LMNB2):c.1554G>C (p.Thr518=)

dbSNP: rs11882908
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001079747 SCV000656054 benign Progressive myoclonic epilepsy type 9; Lipodystrophy, partial, acquired, susceptibility to 2024-02-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000712222 SCV000842660 benign not provided 2017-09-29 criteria provided, single submitter clinical testing
GeneDx RCV000712222 SCV001890063 benign not provided 2021-06-09 criteria provided, single submitter clinical testing

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