Variant (rsID / SNP)
rs370920665
rs370920665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,380,194. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
KRASConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25380194
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.264A>G (p.Lys88=)
- Allele change
- Synonymous_K88K
Associated conditions / phenotypes
Noonan syndrome|RASopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.