List of variants in gene PRNP reported as pathogenic for Huntington disease-like 1

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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: 10

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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.154_177[6_13]	rs193922906
NM_000311.5(PRNP):c.305C>T (p.Pro102Leu)	rs74315401
NM_000311.5(PRNP):c.350_351inv (p.Ala117Val)
NM_000311.5(PRNP):c.392G>T (p.Gly131Val)	rs74315410
NM_000311.5(PRNP):c.478C>T (p.Gln160Ter)	rs80356711
NM_000311.5(PRNP):c.532G>A (p.Asp178Asn)	rs74315403
NM_000311.5(PRNP):c.547A>G (p.Thr183Ala)	rs74315411
NM_000311.5(PRNP):c.593T>C (p.Phe198Ser)	rs74315405
NM_000311.5(PRNP):c.598G>A (p.Glu200Lys)	rs28933385

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