Variant (rsID / SNP)
rs104894366
rs104894366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,398,218. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
KRASPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25398218
- Cytoband
- 12p12.1
- HGVS
- NM_004985.5(KRAS):c.101C>G (p.Pro34Arg)
- Allele change
- Missense_P34R
Associated conditions / phenotypes
Cardiofaciocutaneous syndrome 2|Cardio-facio-cutaneous syndrome|Noonan syndrome|Acute myeloid leukemia|Autoimmune lymphoproliferative syndrome type 4|Cardiofaciocutaneous syndrome 2|Noonan syndrome 3|RASopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.