List of variants in gene VWA1 reported as uncertain significance for Neuronopathy, distal hereditary motor, autosomal recessive 7

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_022834.5(VWA1):c.1121G>A (p.Gly374Glu)
NM_022834.5(VWA1):c.1275GCGCCC[3] (p.Pro431_Val432insArgPro)
NM_022834.5(VWA1):c.1312C>A (p.Pro438Thr)

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