Variant (rsID / SNP)
rs2229247
rs2229247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FDFT1. Location: chromosome 8, position 11,683,622. The table records no clinical significance for this variant.
Reference-table entries
FDFT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 8:11683622
- HGVS
- NM_001287750.2,c.777T>C,p.Asp259Asp
- Allele change
- Synonymous_D200D
Associated conditions / phenotypes
Synonymous_D33D|Synonymous_D136D|Synonymous_D136D|Synonymous_D136D|Synonymous_D259D|Synonymous_D115D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.