List of variants in gene PRNP reported as uncertain significance for Gerstmann-Straussler-Scheinker syndrome

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000311.5(PRNP):c.*115G>A	rs746943389	0.00014
NM_000311.5(PRNP):c.498G>A (p.Met166Ile)	rs745480639	0.00002
NM_000311.5(PRNP):c.695T>G (p.Met232Arg)	rs74315409	0.00002
NM_000311.5(PRNP):c.206A>T (p.His69Leu)

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