Variant (rsID / SNP)
rs2260655
rs2260655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TKFC. Location: chromosome 11, position 61,108,974. The table records no clinical significance for this variant.
Reference-table entries
TKFCNot classified
- Variant type
- missense_variant
- Chromosome / position
- 11:61108974
- HGVS
- NM_001351977.2,c.553G>A,p.Ala185Thr
- Allele change
- Missense_A185T
Associated conditions / phenotypes
Missense_A185T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.