List of variants in gene VMA12 reported as pathogenic for disorder of multiple glycosylation

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152464.3(VMA12):c.92G>C (p.Arg31Pro)	rs782531869	0.00006
NM_152464.3(VMA12):c.376-1G>A	rs869025587
NM_152464.3(VMA12):c.40G>C (p.Ala14Pro)	rs869025586

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