Variant (rsID / SNP)
rs1006030
rs1006030 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGBL1. Location: chromosome 15, position 87,531,281. The table records no clinical significance for this variant.
Reference-table entries
AGBL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:87531281
- HGVS
- NM_152336.4,c.3285A>C,p.Thr1095Thr
- Allele change
- Synonymous_T1095T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
