Variant (rsID / SNP)
rs2053028
rs2053028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT2. Location: chromosome 5, position 150,901,613. The table records no clinical significance for this variant.
Reference-table entries
FAT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:150901613
- HGVS
- NM_001447.3,c.10541T>C,p.Leu3514Ser
- Allele change
- Missense_L3514S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.