Variant (rsID / SNP)
rs778805
rs778805 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT6. Location: chromosome 19, position 5,832,209. Clinical significance in the table: Benign.
Reference-table entries
FUT6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 19:5832209
- HGVS
- NM_000150.4,c.370C>T,p.Pro124Ser
- Allele change
- Missense_P124S
Associated conditions / phenotypes
Fucosyltransferase 6 Deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.