Variant (rsID / SNP)
rs763213
rs763213 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR5. Location: chromosome 22, position 45,075,738. The table records no clinical significance for this variant.
Reference-table entries
PRR5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:45075738
- HGVS
- NM_001198721.2,c.59T>C,p.Met20Thr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.