Variant (rsID / SNP)

rs150039898

rs150039898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPP1. Location: chromosome 11, position 6,636,520. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TPP1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:6636520
Cytoband: 11p15.4
HGVS: NM_000391.4(TPP1):c.1307T>C (p.Leu436Pro)
Allele change: Missense_L436P

Associated conditions / phenotypes

Neuronal ceroid lipofuscinosis|Seizure|Neuronal ceroid lipofuscinosis 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.