List of variants in gene WFS1 reported as pathogenic for Wolfram 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.2369C>A (p.Ser790Ter)	rs369107336
NM_006005.3(WFS1):c.409_424dup (p.Val142fs)	rs1362648752
NM_006005.3(WFS1):c.873C>G (p.Tyr291Ter)	rs777580652

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