List of variants in gene SNCB studied for synucleinopathy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_003085.5(SNCB):c.121+6T>C	rs4868669	0.97242
NM_003085.5(SNCB):c.368C>A (p.Pro123His)	rs104893937	0.00021
NM_003085.5(SNCB):c.208G>A (p.Val70Met)	rs104893936	0.00001
NM_003085.5(SNCB):c.100A>G (p.Lys34Glu)	rs2113420521
NM_003085.5(SNCB):c.269C>T (p.Pro90Leu)
NM_003085.5(SNCB):c.37G>C (p.Glu13Gln)
NM_003085.5(SNCB):c.55G>A (p.Ala19Thr)

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