Variant (rsID / SNP)
rs602662
rs602662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUT2. Location: chromosome 19, position 49,206,985. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 19:49206985
- HGVS
- NM_000511.6,c.772G>A,p.Gly258Ser
- Allele change
- Missense_G258S
Associated conditions / phenotypes
Ulcerative Colitis|Crohn's Disease|Iron Deficiency Anemia|Colitis|Miyoshi Muscular Dystrophy 2|Inflammatory Bowel Disease 1|Deficiency Anemia|Iron Metabolism Disease|Diarrhea|Inflammatory Bowel Disease|Bronchiolitis|Sclerosing Cholangitis|Body Mass Index Quantitative Trait Locus 11|Oral Squamous Cell Carcinoma|Heart Disease|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.