Variant (rsID / SNP)
rs146955208
rs146955208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA. Location: chromosome 1, position 13,480,638. The table records no clinical significance for this variant.
Reference-table entries
NANot classified
- Variant type
- intergenic_region
- Chromosome / position
- 1:13480638
- HGVS
- NA,n.13480638C>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.