ClinVar Miner

List of variants in gene combination MYH11, NDE1 reported as likely benign for visceral myopathy 2

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_002474.3(MYH11):c.4578+19T>C	rs118072250	0.00034
NM_002474.3(MYH11):c.5829A>G (p.Gly1943=)	rs199752132	0.00001

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