Variant (rsID / SNP)
rs2297555
rs2297555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTRF1. Location: chromosome 13, position 41,834,744. The table records no clinical significance for this variant.
Reference-table entries
MTRF1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:41834744
- HGVS
- NM_001354073.1,c.300G>A,p.Glu100Glu
- Allele change
- Synonymous_E100E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.