Variant (rsID / SNP)
rs12320366
rs12320366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KERA. Location: chromosome 12, position 91,449,984. The table records no clinical significance for this variant.
Reference-table entries
KERANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:91449984
- HGVS
- NM_007035.4,c.75G>A,p.Gln25Gln
- Allele change
- Synonymous_Q25Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.