Variant (rsID / SNP)
rs121913527
rs121913527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,378,562. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
KRASConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25378562
- Cytoband
- 12p12.1
- HGVS
- NM_033360.4(KRAS):c.436G>T (p.Ala146Ser)
- Allele change
- Missense_A146T
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.