List of variants in gene APTX reported as likely benign 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_001195248.2(APTX):c.484-12_484-11insG	rs377129152	0.06469
NM_001195248.2(APTX):c.851_852del	rs377365362

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