Variant (rsID / SNP)
rs660339
rs660339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UCP2. Location: chromosome 11, position 73,689,104. Clinical significance in the table: Benign.
Reference-table entries
UCP2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:73689104
- Cytoband
- 11q13.4
- HGVS
- NM_003355.3(UCP2):c.164C>T (p.Ala55Val)
- Allele change
- Missense_A55V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.