Variant (rsID / SNP)
rs3132453
rs3132453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2A. Location: chromosome 6, position 31,604,044. The table records no clinical significance for this variant.
Reference-table entries
PRRC2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31604044
- HGVS
- NM_004638.4,c.5683T>G,p.Leu1895Val
- Allele change
- Missense_L1895V
Associated conditions / phenotypes
Lymphoma, Non-Hodgkin, Familial|Lymphoma, Hodgkin, Classic|B-Cell Lymphoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.