Variant (rsID / SNP)
rs369501492
rs369501492 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,362,788. Clinical significance in the table: Uncertain significance.
Reference-table entries
KRASUncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25362788
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.508A>T (p.Met170Leu)
- Allele change
- Silent
Associated conditions / phenotypes
RASopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.