Variant (rsID / SNP)
rs12443991
rs12443991 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA. Location: chromosome 16, position 85,204,221. The table records no clinical significance for this variant.
Reference-table entries
NANot classified
- Variant type
- intergenic_region
- Chromosome / position
- 16:85204221
- HGVS
- NA,n.85204221C>T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.