Variant (rsID / SNP)

rs1801474

rs1801474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKN. Location: chromosome 6, position 162,622,197. Clinical significance in the table: Benign.

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Reference-table entries

PRKNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:162622197
Cytoband: 6q26
HGVS: NM_004562.3(PRKN):c.500G>A (p.Ser167Asn)
Allele change: Missense_S167N

Associated conditions / phenotypes

Autosomal recessive juvenile Parkinson disease 2

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.