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Variant (rsID / SNP)

rs201771769

ZFYVE26

rs201771769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE26. Location: chromosome 14, position 68,215,361. 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
14:68215361
Cytoband
14q24.1
HGVS
NM_015346.4(ZFYVE26):c.7417-5G>C
Allele change
Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 15|Spastic paraplegia|Hereditary spastic paraplegia

Public references

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