Variant (rsID / SNP)
rs28489284
rs28489284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST3GAL6. Location: chromosome 3, position 98,512,540. The table records no clinical significance for this variant.
Reference-table entries
ST3GAL6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:98512540
- HGVS
- NM_001271145.2,c.1090G>A,p.Ala364Thr
- Allele change
- Missense_A225T
Associated conditions / phenotypes
Missense_A167T|Missense_A311T|Missense_A311T|Missense_A225T|Missense_A203T|Missense_A311T|Missense_A364T|Missense_A167T|Missense_A167T|Missense_A311T|Missense_A225T|Missense_A334T|Missense_A311T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.