ClinVar Miner

Submissions for variant NM_003282.4(TNNI2):c.15+140C>A

gnomAD frequency: 0.20357  dbSNP: rs1877444
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000128662 SCV001947902 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
TNNI2 homepage - Leiden Muscular Dystrophy pages RCV000128662 SCV000172302 not provided not provided no assertion provided not provided

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