Variant (rsID / SNP)
rs2070229
rs2070229 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MX1. Location: chromosome 21, position 42,821,113. The table records no clinical significance for this variant.
Reference-table entries
MX1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:42821113
- HGVS
- NM_001144925.2,c.1323T>C,p.Arg441Arg
- Allele change
- Synonymous_R441R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.