Variant (rsID / SNP)
rs2230126
rs2230126 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAF1C. Location: chromosome 16, position 84,218,565. The table records no clinical significance for this variant.
Reference-table entries
TAF1CNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 16:84218565
- HGVS
- NM_005679.4,c.30A>G,p.Ala10Ala
- Allele change
- Silent
Associated conditions / phenotypes
Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.