Variant (rsID / SNP)
rs11251721
rs11251721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PFKP. Location: chromosome 10, position 3,150,898. The table records no clinical significance for this variant.
Reference-table entries
PFKPNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:3150898
- HGVS
- NM_002627.5,c.876C>T,p.Val292Val
- Allele change
- Synonymous_V123V
Associated conditions / phenotypes
Synonymous_V284V|Synonymous_V254V|Synonymous_V254V|Synonymous_V76V|Synonymous_V76V|Synonymous_V76V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.