ClinVar Miner

List of variants in gene WFS1 reported as uncertain significance for Spastic ataxia

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.1969A>G (p.Met657Val)	rs71532861	0.00010
NM_006005.3(WFS1):c.401C>T (p.Ala134Val)	rs746010848	0.00002

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