ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.864_867del (p.His289fs)

dbSNP: rs60168366
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
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057476 SCV000088590 not provided not provided no assertion provided not provided
Inherited Neuropathy Consortium RCV000790001 SCV000929390 uncertain significance Charcot-Marie-Tooth disease no assertion criteria provided literature only

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