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Variant (rsID / SNP)

rs778986

FUT3

rs778986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT3. Location: chromosome 19, position 5,844,537. The table records no clinical significance for this variant.

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Reference-table entries

FUT3Not classified
Variant type
missense_variant
Chromosome / position
19:5844537
HGVS
NM_000149.4,c.314T>C,p.Met105Thr
Allele change
Missense_M105T

Associated conditions / phenotypes

Immunoglobulin Alpha Deficiency

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.