Variant (rsID / SNP)
rs2391199
rs2391199 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVI5. Location: chromosome 1, position 93,160,902. Clinical significance in the table: Benign.
Reference-table entries
EVI5Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:93160902
- Cytoband
- 1p22.1
- HGVS
- NM_001350197.2(EVI5):c.874A>G (p.Ile292Val)
- Allele change
- Missense_I292V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.