Variant (rsID / SNP)
rs3211098
rs3211098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFF. Location: chromosome 2, position 228,194,481. Clinical significance in the table: Benign.
Reference-table entries
MFFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:228194481
- Cytoband
- 2q36.3
- HGVS
- NM_001277062.2(MFF):c.-40-861G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.