Variant (rsID / SNP)
rs2272593
rs2272593 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2A. Location: chromosome 6, position 31,601,344. The table records no clinical significance for this variant.
Reference-table entries
PRRC2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31601344
- HGVS
- NM_004638.4,c.4508T>C,p.Leu1503Pro
- Allele change
- Missense_L1503P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.