Variant (rsID / SNP)
rs4508712
rs4508712 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKDREJ. Location: chromosome 22, position 46,652,959. The table records no clinical significance for this variant.
Reference-table entries
PKDREJNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:46652959
- HGVS
- NM_006071.2,c.6261T>C,p.Pro2087Pro
- Allele change
- Synonymous_P2087P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
