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Variant (rsID / SNP)

rs34952009

ZFYVE26

rs34952009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE26. Location: chromosome 14, position 68,234,533. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZFYVE26Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:68234533
Cytoband
14q24.1
HGVS
NM_015346.4(ZFYVE26):c.5678G>T (p.Ser1893Ile)
Allele change
Missense_S1893I

Associated conditions / phenotypes

Spastic paraplegia|Hereditary spastic paraplegia 15|Hereditary spastic paraplegia

Public references

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