ClinVar Miner

List of variants reported as likely pathogenic for visceral myopathy 2

Included ClinVar conditions (3):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001040113.2(MYH11):c.5819del (p.Pro1940fs)	rs747392139
NM_002474.3(MYH11):c.2135G>A (p.Arg712Gln)	rs267606902
NM_002474.3(MYH11):c.582C>G (p.Tyr194Ter)

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