Variant (rsID / SNP)
rs56314249
rs56314249 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT1. Location: chromosome 13, position 28,896,979. The table records no clinical significance for this variant.
Reference-table entries
FLT1Not classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:28896979
- Cytoband
- 13q12.3
- HGVS
- NM_002019.4(FLT1):c.2901G>A (p.Ala967=)
- Allele change
- Synonymous_A967A
Associated conditions / phenotypes
Carcinoma of colon
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.