Variant (rsID / SNP)
rs3740617
rs3740617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMO2. Location: chromosome 11, position 33,881,016. The table records no clinical significance for this variant.
Reference-table entries
LMO2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:33881016
- HGVS
- NM_005574.4,c.570A>G,p.Lys190Lys
- Allele change
- Synonymous_K121K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.