ClinVar Miner

List of variants in gene SNCA studied for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NC_000004.11:g.(?_90647315)_(90756828_?)dup
NC_000004.11:g.(?_90647315)_(90756838_?)dup
NM_000345.4(SNCA):c.150T>G (p.His50Gln) rs201106962
NM_000345.4(SNCA):c.152G>A (p.Gly51Asp) rs431905511
NM_000345.4(SNCA):c.157G>A (p.Ala53Thr) rs104893877
NM_000345.4(SNCA):c.349C>A (p.Pro117Thr)
NM_000345.4(SNCA):c.408C>T (p.Tyr136=) rs76642636
NM_000345.4(SNCA):c.88G>C (p.Ala30Pro) rs104893878
SNCA, DUPLICATION
SNCA, TRIPLICATION

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