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Variant (rsID / SNP)

rs140117984

ZFYVE26

rs140117984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE26. Location: chromosome 14, position 68,238,751. 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
14:68238751
Cytoband
14q24.1
HGVS
NM_015346.4(ZFYVE26):c.5484+13G>A
Allele change
Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 15|Spastic paraplegia

Public references

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