ClinVar Miner

List of variants in gene PRNP reported as uncertain significance for Inherited Creutzfeldt-Jakob disease

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000311.5(PRNP):c.623G>A (p.Arg208His)	rs74315412	0.00004
NM_000311.5(PRNP):c.695T>G (p.Met232Arg)	rs74315409	0.00002

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