Variant (rsID / SNP)

rs10883841

rs10883841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NT5C2. Location: chromosome 10, position 104,934,709. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NT5C2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:104934709
Cytoband: 10q24.33
HGVS: NM_001351169.2(NT5C2):c.7A>G (p.Thr3Ala)
Allele change: Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 45

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.