Variant (rsID / SNP)
rs3822699
rs3822699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT2. Location: chromosome 5, position 150,901,111. The table records no clinical significance for this variant.
Reference-table entries
FAT2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 5:150901111
- HGVS
- NM_001447.3,c.11043T>C,p.Asp3681Asp
- Allele change
- Synonymous_D3681D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.