Variant (rsID / SNP)

rs9266

rs9266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,362,217. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KRASBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:25362217
Cytoband: 12p12.1
HGVS: NM_033360.4(KRAS):c.*633T>C
Allele change: Silent

Associated conditions / phenotypes

Noonan syndrome|Noonan syndrome and Noonan-related syndrome

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.