Variant (rsID / SNP)
rs727503111
rs727503111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,403,833. Clinical significance in the table: Benign.
Reference-table entries
KRASBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25403833
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.-160A>G
- Allele change
- Silent
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.