Variant (rsID / SNP)
rs2276528
rs2276528 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDXK. Location: chromosome 21, position 45,152,500. The table records no clinical significance for this variant.
Reference-table entries
PDXKNot classified
- Variant type
- intron_variant
- Chromosome / position
- 21:45152500
- HGVS
- NM_003681.5,c.88-1450G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.