Variant (rsID / SNP)
rs1049814
rs1049814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDLIM1. Location: chromosome 10, position 96,997,820. The table records no clinical significance for this variant.
Reference-table entries
PDLIM1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:96997820
- HGVS
- NM_020992.4,c.852T>C,p.Tyr284Tyr
- Allele change
- Synonymous_Y284Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.