List of variants in gene PRNP reported as likely benign for inherited Creutzfeldt-Jakob disease

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000311.5(PRNP):c.385A>G (p.Met129Val)	rs1799990	0.33516
NM_000311.5(PRNP):c.306G>A (p.Pro102=)	rs370426100	0.00012
NM_000311.5(PRNP):c.159C>T (p.Gly53=)	rs776188950	0.00004
NM_000311.5(PRNP):c.636G>A (p.Gln212=)	rs757784308	0.00002
NM_000311.3(PRNP):c.204_227del24 (p.Pro84_Gln91del)	rs193922906

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