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Variant (rsID / SNP)

rs386833642

PPT1

rs386833642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPT1. Location: chromosome 1, position 40,557,754. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PPT1Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
1:40557754
Cytoband
1p34.2
HGVS
NM_000310.4(PPT1):c.325T>G (p.Tyr109Asp)
Allele change
Missense_Y109D

Associated conditions / phenotypes

Neuronal ceroid lipofuscinosis 1

Public references

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