Variant (rsID / SNP)
rs37458
rs37458 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST3GAL3. Location: chromosome 1, position 44,290,530. Clinical significance in the table: Benign.
Reference-table entries
ST3GAL3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:44290530
- Cytoband
- 1p34.1
- HGVS
- NM_006279.5(ST3GAL3):c.209+9925A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.