Variant (rsID / SNP)
rs104886029
rs104886029 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,380,282. The table records no clinical significance for this variant.
Reference-table entries
KRASNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:25380282
- Cytoband
- 12p12.1
- HGVS
- NM_033360.4(KRAS):c.176C>T (p.Ala59Val)
- Allele change
- Missense_A59V
Associated conditions / phenotypes
Familial cancer of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.