Variant (rsID / SNP)
rs587782087
rs587782087 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,061,895. Clinical significance in the table: Uncertain significance.
Reference-table entries
MLH1Uncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:37061895
- Cytoband
- 3p22.2
- HGVS
- NM_000249.4(MLH1):c.979C>G (p.Gln327Glu)
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms|Colorectal cancer, hereditary nonpolyposis, type 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.