Variant (rsID / SNP)
rs7993418
rs7993418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT1. Location: chromosome 13, position 28,883,061. The table records no clinical significance for this variant.
Reference-table entries
FLT1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:28883061
- HGVS
- NM_002019.4,c.3639C>T,p.Tyr1213Tyr
- Allele change
- Synonymous_Y1213Y
Associated conditions / phenotypes
Renal Cell Carcinoma, Nonpapillary|Type 2 Diabetes Mellitus|Microvascular Complications of Diabetes 5|Kuhnt-Junius Degeneration|Macular Degeneration, Age-Related, 1|Colorectal Cancer|Pancreatic Adenocarcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.