ClinVar Miner

Submissions for variant NM_005857.5(ZMPSTE24):c.357+114A>G

gnomAD frequency: 0.25626  dbSNP: rs7516571
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
GeneDx RCV000128739 SCV001858202 benign not provided 2018-11-13 criteria provided, single submitter clinical testing
ZMPSTE24 homepage - Leiden Muscular Dystrophy pages RCV000128739 SCV000172379 not provided not provided no assertion provided not provided

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