List of variants in gene PDE8B reported as likely benign for synucleinopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_003719.5(PDE8B):c.*1265G>A	rs138511945	0.00085
NM_003719.5(PDE8B):c.*30G>A	rs201812762	0.00015
NM_003719.5(PDE8B):c.1317G>A (p.Pro439=)	rs754763694	0.00010
NM_003719.5(PDE8B):c.1107-6T>A	rs367814038	0.00005
NM_003719.5(PDE8B):c.2343C>T (p.Asp781=)	rs558853134	0.00004
NM_003719.5(PDE8B):c.796C>T (p.Arg266Trp)	rs375768747	0.00003
NM_003719.5(PDE8B):c.1881C>T (p.Thr627=)	rs143919281	0.00002
NM_003719.5(PDE8B):c.876+15C>T	rs756229238	0.00002
NM_003719.5(PDE8B):c.1031T>G (p.Val344Gly)	rs767230883

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