Variant (rsID / SNP)
rs2230004
rs2230004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETS1. Location: chromosome 11, position 128,333,503. The table records no clinical significance for this variant.
Reference-table entries
ETS1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:128333503
- HGVS
- NM_001143820.2,c.1143A>G,p.Leu381Leu
- Allele change
- Synonymous_L250L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
