List of variants in gene SAMD9L reported as uncertain significance for Spinocerebellar ataxia 49

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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_152703.5(SAMD9L):c.3932A>T (p.Asp1311Val)
NM_152703.5(SAMD9L):c.4140dup (p.Gln1381fs)	rs745823605
NM_152703.5(SAMD9L):c.499C>A (p.Pro167Thr)
NM_152703.5(SAMD9L):c.683G>A (p.Cys228Tyr)	rs1433514195

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