ClinVar Miner

List of variants reported as uncertain significance for Lewy body dementia by Invitae

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 20
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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.391-7A>G rs2110065158
NM_000345.4(SNCA):c.401A>G (p.Gln134Arg)
NM_000345.4(SNCA):c.47T>C (p.Val16Ala) rs1289802008

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