Variant (rsID / SNP)
rs6025606
rs6025606 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTCFL. Location: chromosome 20, position 56,098,733. The table records no clinical significance for this variant.
Reference-table entries
CTCFLNot classified
- Variant type
- missense_variant
- Chromosome / position
- 20:56098733
- HGVS
- NM_001269043.2,c.529A>G,p.Thr177Ala
- Allele change
- Missense_T177A
Associated conditions / phenotypes
Missense_T177A|Silent|Missense_T177A|Silent|Silent|Missense_T177A|Silent|Missense_T177A|Missense_T177A|Missense_T177A|Missense_T177A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.