List of variants in gene SNCA reported as likely benign for Lewy body dementia; Autosomal dominant Parkinson disease 1; Autosomal dominant Parkinson disease 4

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000345.4(SNCA):c.*139T>G	rs10024743	0.00703
NM_000345.4(SNCA):c.121+11C>T	rs35135226	0.00022
NM_000345.4(SNCA):c.391-16A>G	rs371014092	0.00006
NM_000345.4(SNCA):c.*77C>A	rs145304567
NM_000345.4(SNCA):c.243A>G (p.Thr81=)	rs568436589

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