Variant (rsID / SNP)
rs3219485
rs3219485 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUTYH. Location: chromosome 1, position 45,800,033. Clinical significance in the table: Benign.
Reference-table entries
MUTYHBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:45800033
- Cytoband
- 1p34.1
- HGVS
- NM_001048174.2(MUTYH):c.115+30A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.