Variant (rsID / SNP)

rs1127745

rs1127745 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOX2. Location: chromosome 3, position 58,512,237. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ACOX2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:58512237
HGVS: NM_003500.4,c.1302T>C,p.Cys434Cys
Allele change: Synonymous_C434C

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.