ClinVar Miner

List of variants in gene LYST 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_000081.4(LYST):c.4336C>T (p.Arg1446Trp)	rs200276917	0.00010
NM_000081.4(LYST):c.5590G>T (p.Val1864Leu)	rs139694536

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