ClinVar Miner

List of variants in gene INSR reported as likely benign for Bailey-Bloch congenital myopathy

Included ClinVar conditions (1):

Bailey-Bloch congenital myopathy

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.3034G>A (p.Val1012Met)	rs1799816	0.00500

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