Variant (rsID / SNP)
rs492602
rs492602 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT2. Location: chromosome 19, position 49,206,417. The table records no clinical significance for this variant.
Reference-table entries
FUT2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:49206417
- HGVS
- NM_000511.6,c.204A>G,p.Ala68Ala
- Allele change
- Synonymous_A68A
Associated conditions / phenotypes
Patent Ductus Venosus|Psoriasis 1|Vitamin B12 Plasma Level Quantitative Trait Locus 1|Pustulosis of Palm and Sole|Psoriasis|Hemochromatosis, Type 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.