ClinVar Miner

List of variants reported as uncertain significance for striatal degeneration, autosomal dominant by Centre for Mendelian Genomics, University Medical Centre Ljubljana

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003719.5(PDE8B):c.1576+4A>G	rs1794602797
NM_003719.5(PDE8B):c.2649dup (p.Asp884Ter)	rs1798184496
NM_003719.5(PDE8B):c.878A>G (p.Tyr293Cys)	rs1780697407

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