Variant (rsID / SNP)

rs7135947

rs7135947 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACACB. Location: chromosome 12, position 109,629,457. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ACACBNot classified

Variant type: synonymous_variant
Chromosome / position: 12:109629457
HGVS: NM_001093.4,c.2184C>T,p.Gly728Gly
Allele change: Synonymous_G728G

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.