Variant (rsID / SNP)
rs539351
rs539351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCNT2. Location: chromosome 6, position 10,587,038. The table records no clinical significance for this variant.
Reference-table entries
GCNT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:10587038
- HGVS
- NM_145655.4,c.816C>G,p.Asp272Glu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.