Variant (rsID / SNP)
rs77086855
rs77086855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEFV. Location: chromosome 16, position 3,299,015. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
MEFVConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:3299015
- Cytoband
- 16p13.3
- HGVS
- NM_000243.3(MEFV):c.1261-11T>G
- Allele change
- Silent
Associated conditions / phenotypes
Familial Mediterranean fever
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.