List of variants in gene SNCA reported as uncertain significance for basal ganglia disorder

Minimum submission review status:		Collection method:
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: 22

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HGVS	dbSNP	gnomAD frequency
NM_000345.4(SNCA):c.349C>A (p.Pro117Thr)	rs145138372	0.00016
NM_000345.4(SNCA):c.150T>G (p.His50Gln)	rs201106962	0.00007
NM_000345.4(SNCA):c.*464C>A	rs183204610	0.00002
NM_000345.4(SNCA):c.359C>T (p.Pro120Leu)	rs1024288001	0.00001
NM_000345.4(SNCA):c.382C>A (p.Pro128Thr)	rs750899874	0.00001
NM_000345.4(SNCA):c.71A>G (p.Gln24Arg)	rs1739236610	0.00001
NC_000004.11:g.(?_90647315)_(90756828_?)del
NM_000345.4(SNCA):c.100A>G (p.Lys34Glu)	rs1330229174
NM_000345.4(SNCA):c.122-2A>C	rs2110488615
NM_000345.4(SNCA):c.158C>T (p.Ala53Val)	rs542171324
NM_000345.4(SNCA):c.163+6C>A	rs2110488377
NM_000345.4(SNCA):c.203G>A (p.Gly68Glu)
NM_000345.4(SNCA):c.217G>A (p.Gly73Ser)
NM_000345.4(SNCA):c.247G>C (p.Glu83Gln)	rs2110460484
NM_000345.4(SNCA):c.31G>T (p.Ala11Ser)
NM_000345.4(SNCA):c.342A>C (p.Glu114Asp)
NM_000345.4(SNCA):c.367G>A (p.Glu123Lys)
NM_000345.4(SNCA):c.391-14T>C
NM_000345.4(SNCA):c.391-7A>G	rs2110065158
NM_000345.4(SNCA):c.401A>G (p.Gln134Arg)
NM_000345.4(SNCA):c.47T>C (p.Val16Ala)	rs1289802008
NM_000345.4(SNCA):c.89C>G (p.Ala30Gly)	rs2110525413

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