Variant (rsID / SNP)
rs2421847
rs2421847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2C. Location: chromosome 1, position 171,557,600. The table records no clinical significance for this variant.
Reference-table entries
PRRC2CNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:171557600
- HGVS
- NM_001387844.1,c.8155A>G,p.Thr2719Ala
- Allele change
- Missense_T2717A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.