Variant (rsID / SNP)
rs2303633
rs2303633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SART3. Location: chromosome 12, position 108,918,146. The table records no clinical significance for this variant.
Reference-table entries
SART3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:108918146
- HGVS
- NM_014706.4,c.2661G>A,p.Pro887Pro
- Allele change
- Synonymous_P887P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.