Variant (rsID / SNP)

rs150351644

rs150351644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRNP. Location: chromosome 20, position 4,680,290. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PRNPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:4680290
Cytoband: 20p13
HGVS: NM_000311.5(PRNP):c.424G>A (p.Gly142Ser)
Allele change: Silent

Associated conditions / phenotypes

Inherited prion disease|Huntington disease-like 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.