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Variant (rsID / SNP)

rs864622094

SPG7

rs864622094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPG7. Location: chromosome 16, position 89,620,349. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

SPG7Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
16:89620349
Cytoband
16q24.3
HGVS
NM_003119.4(SPG7):c.2084T>C (p.Leu695Pro)
Allele change
Missense_L695P

Associated conditions / phenotypes

Hereditary spastic paraplegia 7

Public references

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