Variant (rsID / SNP)
rs2281820
rs2281820 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLN. Location: chromosome 6, position 33,768,897. The table records no clinical significance for this variant.
Reference-table entries
MLNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:33768897
- HGVS
- NM_002418.3,c.44T>C,p.Val15Ala
- Allele change
- Missense_V15A
Associated conditions / phenotypes
Ampulla of Vater Cancer|Gallbladder Disease 1|Bile Duct Cancer|Constipation|Cholecystitis|Biliary Tract Cancer|Depression
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.