Variant (rsID / SNP)
rs397517476
rs397517476 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,368,449. Clinical significance in the table: Likely benign.
Reference-table entries
KRASLikely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25368449
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.451-5604T>A
- Allele change
- Missense_Y166N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.