Variant (rsID / SNP)
rs10484558
rs10484558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BAG6. Location: chromosome 6, position 31,615,514. The table records no clinical significance for this variant.
Reference-table entries
BAG6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31615514
- HGVS
- NM_001388012.1,c.642A>G,p.Thr214Thr
- Allele change
- Synonymous_T214T
Associated conditions / phenotypes
Synonymous_T214T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.