Variant (rsID / SNP)
rs1800797
rs1800797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL6. Location: chromosome 7, position 22,766,221. Clinical significance in the table: Benign.
Reference-table entries
IL6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:22766221
- Cytoband
- 7p15.3
- HGVS
- NR_131935.1(IL6-AS1):n.157T>C
- Allele change
- Silent
Associated conditions / phenotypes
INTERLEUKIN 6 POLYMORPHISM
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.