ClinVar Miner

List of variants reported as uncertain significance for autosomal recessive spastic ataxia by New York Genome Center

Included ClinVar conditions (9):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.1033C>T (p.Arg345Trp)	rs776156836	0.00011
NM_014363.6(SACS):c.110G>A (p.Arg37His)	rs866539724	0.00006

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