Variant (rsID / SNP)
rs2228043
rs2228043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL6ST. Location: chromosome 5, position 55,251,931. The table records no clinical significance for this variant.
Reference-table entries
IL6STNot classified
- Variant type
- missense_variant
- Chromosome / position
- 5:55251931
- HGVS
- NM_002184.4,c.1189C>G,p.Leu397Val
- Allele change
- Missense_L397V
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Multiple Sclerosis|Silent|Missense_L397V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.