Variant (rsID / SNP)
rs10823171
rs10823171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PBLD. Location: chromosome 10, position 70,051,928. The table records no clinical significance for this variant.
Reference-table entries
PBLDNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:70051928
- HGVS
- NM_022129.4,c.351T>C,p.Asp117Asp
- Allele change
- Synonymous_D117D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.