Variant (rsID / SNP)
rs1800795
rs1800795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL6. Location: chromosome 7, position 22,766,645. Clinical significance in the table: risk factor.
Reference-table entries
IL6Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:22766645
- Cytoband
- 7p15.3
- HGVS
- NG_011640.1:g.4880C>G
- Allele change
- Silent
Associated conditions / phenotypes
Kaposi sarcoma|Crohn disease-associated growth failure, susceptibility to|Intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to|Rheumatoid arthritis, systemic juvenile, susceptibility to|Diabetes mellitus type 2, susceptibility to|Diabetes mellitus, type 1, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.