Variant (rsID / SNP)
rs2295281
rs2295281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFN2. Location: chromosome 1, position 12,059,412. Clinical significance in the table: Benign.
Reference-table entries
MFN2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:12059412
- Cytoband
- 1p36.22
- HGVS
- NM_014874.4(MFN2):c.816+260C>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.