ClinVar Miner

List of variants reported as not provided for myopathy, centronuclear, 2 by GenomeConnect - Invitae Patient Insights Network

Included ClinVar conditions (2):

Myopathy, centronuclear, 2
Primary dilated cardiomyopathy; Myopathy, centronuclear, 2; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_139343.3(BIN1):c.696C>A (p.Asn232Lys)	rs143820618	0.00034
NM_001267550.2(TTN):c.34930+2T>C	rs749252830	0.00004

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