Variant (rsID / SNP)
rs2230283
rs2230283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT4. Location: chromosome 12, position 89,916,811. The table records no clinical significance for this variant.
Reference-table entries
GALNT4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:89916811
- HGVS
- NM_003774.5,c.1516G>A,p.Val506Ile
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.