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Variant (rsID / SNP)

rs35077384

ZFYVE27

rs35077384 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE27. Location: chromosome 10, position 99,509,251. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZFYVE27Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:99509251
Cytoband
10q24.2
HGVS
NM_001385875.1(ZFYVE27):c.572G>T (p.Gly191Val)
Allele change
Missense_G93V

Associated conditions / phenotypes

Hereditary spastic paraplegia 33|Spastic tetraparesis|Spastic paraplegia

Public references

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