Variant (rsID / SNP)
rs10745623
rs10745623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EEA1. Location: chromosome 12, position 93,196,422. The table records no clinical significance for this variant.
Reference-table entries
EEA1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:93196422
- HGVS
- NM_003566.4,c.2428A>C,p.Lys810Gln
- Allele change
- Missense_K810Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.