Variant (rsID / SNP)
rs1356410
rs1356410 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G4F. Location: chromosome 15, position 42,434,837. The table records no clinical significance for this variant.
Reference-table entries
PLA2G4FNot classified
- Variant type
- missense_variant
- Chromosome / position
- 15:42434837
- HGVS
- NM_213600.4,c.2218A>G,p.Met740Val
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.