Variant (rsID / SNP)
rs4602367
rs4602367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCL2. Location: chromosome 3, position 17,053,499. The table records no clinical significance for this variant.
Reference-table entries
PLCL2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:17053499
- HGVS
- NM_001144382.2,c.2661A>G,p.Gly887Gly
- Allele change
- Missense_K884E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.