Variant (rsID / SNP)
rs112115496
rs112115496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST3GAL6. Location: chromosome 3, position 98,503,792. The table records no clinical significance for this variant.
Reference-table entries
ST3GAL6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:98503792
- HGVS
- NM_001271145.2,c.498A>G,p.Ile166Met
- Allele change
- Missense_I27M
Associated conditions / phenotypes
Missense_I113M|Missense_I113M|Missense_I27M|Missense_I5M|Missense_I113M|Missense_I166M|Silent|Missense_I113M|Missense_I27M|Missense_I136M|Missense_I113M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.