Variant (rsID / SNP)
rs104895245
rs104895245 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF1A. Location: chromosome 12, position 6,442,960. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
TNFRSF1AConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:6442960
- Cytoband
- 12p13.31
- HGVS
- NM_001065.4(TNFRSF1A):c.265T>C (p.Phe89Leu)
- Allele change
- Silent
Associated conditions / phenotypes
TNF receptor-associated periodic fever syndrome (TRAPS)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.