List of variants in gene MGP reported as pathogenic for Keutel syndrome

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000900.5(MGP):c.62-2A>G	rs112518413	0.00001
NM_000900.5(MGP):c.43del (p.Ala14_Val15insTer)	rs730880321
NM_000900.5(MGP):c.87T>A (p.Tyr29Ter)	rs730880322
NM_000900.5(MGP):c.94+1G>A	rs111320759

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