Variant (rsID / SNP)
rs2228604
rs2228604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORT1. Location: chromosome 1, position 109,884,775. The table records no clinical significance for this variant.
Reference-table entries
SORT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:109884775
- HGVS
- NM_002959.7,c.969A>C,p.Thr323Thr
- Allele change
- Synonymous_T323T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
