ClinVar Miner

List of variants in gene PRNP reported as likely pathogenic 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.538G>A (p.Val180Ile)	rs74315408	0.00003
NM_000311.5(PRNP):c.443G>A (p.Arg148His)	rs181348299	0.00001

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