Variant (rsID / SNP)
rs778971
rs778971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT5. Location: chromosome 19, position 5,867,748. The table records no clinical significance for this variant.
Reference-table entries
FUT5Not classified
- Variant type
- splice_region_variant
- Chromosome / position
- 19:5867748
- HGVS
- NM_002034.2,c.-12C>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
