List of variants in gene SNX14 reported as not provided for cerebellar degeneration

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_153816.6(SNX14):c.1108G>T (p.Glu370Ter)	rs201128942	0.00004
NM_153816.6(SNX14):c.2557+1G>A	rs200277996

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