Variant (rsID / SNP)

rs60488729

rs60488729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPG7. Location: chromosome 16, position 89,617,008. Clinical significance in the table: Benign.

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Reference-table entries

SPG7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:89617008
Cytoband: 16q24.3
HGVS: NM_003119.4(SPG7):c.1770C>T (p.Ala590_Val591=)
Allele change: Synonymous_A590A

Associated conditions / phenotypes

Hereditary spastic paraplegia 7|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.