Variant (rsID / SNP)

rs4830842

rs4830842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATXN3L. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ATXN3LNot classified

Variant type: missense_variant
HGVS: NM_001135995.2,c.995G>A,p.Gly332Asp
Allele change: Silent

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.