List of variants in gene PLD3 reported as uncertain significance for autosomal dominant cerebellar ataxia

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012268.4(PLD3):c.923T>C (p.Leu308Pro)	rs537053537	0.00001
NM_012268.4(PLD3):c.602A>T (p.His201Leu)
NM_012268.4(PLD3):c.615G>A (p.Trp205Ter)	rs2079032507

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