Variant (rsID / SNP)
rs6709462
rs6709462 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PASK. Location: chromosome 2, position 242,082,262. The table records no clinical significance for this variant.
Reference-table entries
PASKNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:242082262
- HGVS
- NM_001252119.2,c.186A>G,p.Thr62Thr
- Allele change
- Synonymous_T62T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
