List of variants in gene combination LOC126860792, PMPCA reported as uncertain significance for Autosomal recessive spinocerebellar ataxia 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015160.3(PMPCA):c.803G>A (p.Arg268Gln)	rs758146224	0.00011
NM_015160.3(PMPCA):c.634-266T>G	rs755207442
NM_015160.3(PMPCA):c.667C>T (p.Arg223Cys)
NM_015160.3(PMPCA):c.802C>T (p.Arg268Trp)

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