Variant (rsID / SNP)

rs141035224

rs141035224 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPG11. Location: chromosome 15, position 44,862,776. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPG11Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:44862776
Cytoband: 15q21.1
HGVS: NM_025137.4(SPG11):c.6424G>A (p.Ala2142Thr)
Allele change: Missense_A2029T

Associated conditions / phenotypes

Hereditary spastic paraplegia 11

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.