Variant (rsID / SNP)
rs8106
rs8106 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP5MC3. Location: chromosome 2, position 176,043,097. Clinical significance in the table: Benign.
Reference-table entries
ATP5MC3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:176043097
- Cytoband
- 2q31.1
- HGVS
- NM_001689.5(ATP5MC3):c.348T>C (p.Tyr116=)
- Allele change
- Synonymous_Y116Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.