Variant (rsID / SNP)
rs1539096
rs1539096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARP4. Location: chromosome 13, position 25,075,859. The table records no clinical significance for this variant.
Reference-table entries
PARP4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:25075859
- HGVS
- NM_006437.4,c.246G>A,p.Arg82Arg
- Allele change
- Synonymous_R82R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.