Variant (rsID / SNP)

rs117666541

rs117666541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AP5Z1. Location: chromosome 7, position 4,825,945. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AP5Z1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:4825945
Cytoband: 7p22.1
HGVS: NM_014855.3(AP5Z1):c.1197G>A (p.Glu399=)
Allele change: Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 48|Hereditary spastic paraplegia

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.