Variant (rsID / SNP)

rs1047781

rs1047781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT2. Location: chromosome 19, position 49,206,631. Clinical significance in the table: Benign; confers sensitivity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FUT2Benign

Clinical significance (as recorded): Benign; confers sensitivity
Variant type: single nucleotide variant
Chromosome / position: 19:49206631
Cytoband: 19q13.33
HGVS: NM_000511.6(FUT2):c.418A>T (p.Ile140Phe)
Allele change: Missense_I140F

Associated conditions / phenotypes

SECRETOR/NONSECRETOR POLYMORPHISM, JAPANESE TYPE|Familial Otitis Media

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.