ClinVar Miner

List of variants in gene WFS1 reported as likely pathogenic for Wolfram syndrome 1; Wolfram-like 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006005.3(WFS1):c.124C>T (p.Arg42Ter)	rs71530923	0.00013
NM_006005.3(WFS1):c.1922C>A (p.Thr641Lys)	rs376626985

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