List of variants in gene SNCA reported as benign by Illumina Laboratory Services, Illumina

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000345.4(SNCA):c.*893C>T	rs356165	0.53603
NM_000345.4(SNCA):c.*2108A>T	rs1045722	0.23733
NM_000345.4(SNCA):c.*2105G>A	rs3857053	0.23489
NM_000345.4(SNCA):c.*1287G>A	rs377356638	0.15186
NM_000345.4(SNCA):c.*501C>T	rs17016074	0.04776
NM_000345.4(SNCA):c.*1677C>T	rs17016072	0.04338
NM_000345.4(SNCA):c.*139T>G	rs10024743	0.00703
NM_000345.4(SNCA):c.*173G>A	rs79726680	0.00645
NM_000345.4(SNCA):c.*1896C>T	rs186189862	0.00484
NM_000345.4(SNCA):c.*593C>A	rs35101723	0.00475
NM_000345.4(SNCA):c.*1002T>G	rs182722435	0.00363
NM_000345.4(SNCA):c.*2230G>A	rs183802441	0.00323
NM_000345.4(SNCA):c.408C>T (p.Tyr136=)	rs76642636	0.00252
NM_000345.4(SNCA):c.121+11C>T	rs35135226	0.00022
NM_000345.4(SNCA):c.*894G>A	rs192179063	0.00011
NM_000345.4(SNCA):c.287A>G (p.Lys96Arg)	rs548523899	0.00003
NM_000345.4(SNCA):c.*249G>A	rs553599518	0.00001
NM_000345.4(SNCA):c.*1260CT[7]	rs5860180
NM_000345.4(SNCA):c.243A>G (p.Thr81=)	rs568436589

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