Variant (rsID / SNP)
rs2070845
rs2070845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFIT2. Location: chromosome 10, position 91,066,075. The table records no clinical significance for this variant.
Reference-table entries
IFIT2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:91066075
- HGVS
- NM_001547.5,c.362A>G,p.Lys121Arg
- Allele change
- Missense_K121R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.