Variant (rsID / SNP)
rs121434568
rs121434568 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EGFR. Location: chromosome 7, position 55,259,515. Clinical significance in the table: drug response.
Reference-table entries
EGFRDrug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:55259515
- Cytoband
- 7p11.2
- HGVS
- NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg)
- Allele change
- Missense_L813R
Associated conditions / phenotypes
Adenocarcinoma of lung, response to tyrosine kinase inhibitor in, somatic|Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic|Tyrosine kinase inhibitor response|gefitinib response - Efficacy|Lung adenocarcinoma|Non-small cell lung carcinoma|Lung carcinoma|Gefitinib response|Erlotinib response
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.