Variant (rsID / SNP)
rs4362360
rs4362360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGBL1. Location: chromosome 15, position 86,940,622. The table records no clinical significance for this variant.
Reference-table entries
AGBL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:86940622
- HGVS
- NM_001386094.1,c.2400T>C,p.Thr800Thr
- Allele change
- Synonymous_T800T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
