List of variants in gene CWF19L1 reported as uncertain significance for cerebellar degeneration

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_018294.6(CWF19L1):c.1045T>G (p.Cys349Gly)	rs1846515941
NM_018294.6(CWF19L1):c.1063A>G (p.Lys355Glu)	rs1176487325
NM_018294.6(CWF19L1):c.1394C>T (p.Ala465Val)	rs2493141272
NM_018294.6(CWF19L1):c.62T>C (p.Leu21Ser)
NM_018294.6(CWF19L1):c.779A>G (p.Asp260Gly)

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