Variant (rsID / SNP)

rs141482368

rs141482368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPP1. Location: chromosome 11, position 6,637,588. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TPP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:6637588
Cytoband: 11p15.4
HGVS: NM_000391.4(TPP1):c.1033A>C (p.Met345Leu)
Allele change: Missense_M345L

Associated conditions / phenotypes

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.