Variant (rsID / SNP)
rs1800693
rs1800693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF1A. Location: chromosome 12, position 6,440,009. Clinical significance in the table: Benign.
Reference-table entries
TNFRSF1ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:6440009
- Cytoband
- 12p13.31
- HGVS
- NM_001065.4(TNFRSF1A):c.625+10A>G
- Allele change
- Silent
Associated conditions / phenotypes
Multiple sclerosis, susceptibility to, 5|TNF receptor-associated periodic fever syndrome (TRAPS)|Susceptibility to severe coronavirus disease (COVID-19)|Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR6|Autoinflammatory syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.