Variant (rsID / SNP)
rs104894362
rs104894362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,362,828. Clinical significance in the table: Pathogenic.
Reference-table entries
KRASPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25362828
- Cytoband
- 12p12.1
- HGVS
- NM_033360.4(KRAS):c.*22C>G
- Allele change
- Silent
Associated conditions / phenotypes
Cardiofaciocutaneous syndrome 2|RASopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.