Variant (rsID / SNP)

rs812936

rs812936 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT3. Location: chromosome 19, position 5,844,649. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FUT3Not classified

Variant type: missense_variant
Chromosome / position: 19:5844649
HGVS: NM_000149.4,c.202C>T,p.Arg68Trp
Allele change: Missense_R68W

Associated conditions / phenotypes

Inflammatory Spondylopathy|Spondyloarthropathy 1|Inflammatory Bowel Disease|Spondylitis|Immunoglobulin Alpha Deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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