List of variants in gene SNCA reported as pathogenic 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000345.4(SNCA):c.150T>G (p.His50Gln)	rs201106962	0.00007
GRCh37/hg19 4q22.1(chr4:90647764-90758128)
NC_000004.11:g.(?_90647315)_(90756828_?)dup
NC_000004.11:g.(?_90647315)_(90756838_?)dup
NC_000004.11:g.(?_90647779)_(90756818_?)dup
NM_000345.4(SNCA):c.136G>A (p.Glu46Lys)	rs104893875
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.88G>C (p.Ala30Pro)	rs104893878
NM_000345.4(SNCA):c.89C>G (p.Ala30Gly)	rs2110525413

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