Variant (rsID / SNP)
rs1800629
rs1800629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNF. Location: chromosome 6, position 31,543,031. Clinical significance in the table: drug response.
Reference-table entries
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:31543031
- Cytoband
- 6p21.33
- HGVS
- NM_000594.3(TNF):c.-488G>A
Associated conditions / phenotypes
etanercept response - Efficacy|Susceptibility to severe coronavirus disease (COVID-19)|Human immunodeficiency virus dementia, susceptibility to|Psoriatic arthritis, susceptibility to|Migraine without aura, susceptibility to|Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR4|Endometriosis|Systemic lupus erythematosus, susceptibility to|Inherited susceptibility to asthma|Malaria, cerebral, susceptibility to|Septic shock, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.