Variant (rsID / SNP)
rs4440995
rs4440995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAX6. Location: chromosome 11, position 31,838,128. The table records no clinical significance for this variant.
Reference-table entries
PAX6Not classified
- Variant type
- upstream_gene_variant
- Chromosome / position
- 11:31838128
- HGVS
- NM_001368887.2,c.-5089C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.