Variant (rsID / SNP)
rs71539626
rs71539626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA. Location: chromosome 19, position 20,481,234. The table records no clinical significance for this variant.
Reference-table entries
NANot classified
- Variant type
- intergenic_region
- Chromosome / position
- 19:20481234
- HGVS
- NA,n.20481234C>T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.