Variant (rsID / SNP)
rs7169981
rs7169981 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX11A. Location: chromosome 15, position 90,226,947. The table records no clinical significance for this variant.
Reference-table entries
PEX11ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:90226947
- HGVS
- NM_003847.3,c.405G>T,p.Leu135Leu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.