Variant (rsID / SNP)

rs17108378

rs17108378 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFYVE27. Location: chromosome 10, position 99,502,897. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZFYVE27Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:99502897
Cytoband: 10q24.2
HGVS: NM_001385875.1(ZFYVE27):c.244G>A (p.Val82Ile)
Allele change: Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 33|Spastic paraplegia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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