C1859298[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1220620	NM_015160.3(PMPCA):c.90C>T (p.Tyr30=)	PMPCA	Single nucleotide variant (5 prime UTR variant +1 more)	Autosomal recessive spinocerebellar ataxia 2 +1 more	GBenign
Select item 1295437	NM_015160.3(PMPCA):c.1200+33G>A	PMPCA	Single nucleotide variant (intron variant)	Autosomal recessive spinocerebellar ataxia 2 +1 more	GBenign