List of variants in gene PMPCA reported as benign for cerebellar 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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015160.3(PMPCA):c.1200+33G>A	rs4604565	0.21146
NM_015160.3(PMPCA):c.90C>T (p.Tyr30=)	rs10870144	0.13348

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