Variant (rsID / SNP)
rs7216955
rs7216955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA. Location: chromosome 17, position 54,123,450. The table records no clinical significance for this variant.
Reference-table entries
NANot classified
- Variant type
- intergenic_region
- Chromosome / position
- 17:54123450
- HGVS
- NA,n.54123450A>G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.