ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_000311.3(PRNP):c.204_227del24 (p.Pro84_Gln91del) rs193922906
NM_000311.5(PRNP):c.159C>T (p.Gly53=) rs776188950
NM_000311.5(PRNP):c.160G>A (p.Gly54Ser) rs763524380
NM_000311.5(PRNP):c.228C>T (p.Pro76=) rs112637437
NM_000311.5(PRNP):c.246_269del (p.60_67PHGGGWGQ[3]) rs138688873
NM_000311.5(PRNP):c.519C>T (p.Asn173=) rs149726579

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