Variant (rsID / SNP)

rs386833635

rs386833635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPT1. Location: chromosome 1, position 40,558,129. Clinical significance in the table: Pathogenic.

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Reference-table entries

PPT1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 1:40558129
Cytoband: 1p34.2
HGVS: NM_000310.4(PPT1):c.175del (p.Glu59fs)

Associated conditions / phenotypes

Neuronal ceroid lipofuscinosis 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.