Variant (rsID / SNP)

rs11979255

rs11979255 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EGFR. Location: chromosome 7, position 55,155,988. The table records no clinical significance for this variant.

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Reference-table entries

EGFRNot classified

Variant type: intron_variant
Chromosome / position: 7:55155988
HGVS: NM_005228.5,c.89-53991G>A
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.