Variant (rsID / SNP)
rs712830
rs712830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EGFR. Location: chromosome 7, position 55,086,780. Clinical significance in the table: Benign.
Reference-table entries
EGFRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:55086780
- Cytoband
- 7p11.2
- HGVS
- NM_005228.5(EGFR):c.-191A>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.