Variant (rsID / SNP)
rs8087447
rs8087447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC35G4. Location: chromosome 18, position 11,609,904. The table records no clinical significance for this variant.
Reference-table entries
SLC35G4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:11609904
- HGVS
- NM_001282300.2,c.310A>G,p.Thr104Ala
- Allele change
- Missense_T104A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.