Variant (rsID / SNP)
rs267607871
rs267607871 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,090,006. Clinical significance in the table: Likely pathogenic.
Reference-table entries
MLH1Likely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:37090006
- Cytoband
- 3p22.2
- HGVS
- NM_000249.4(MLH1):c.1897-2A>G
- Allele change
- Silent
Associated conditions / phenotypes
Lynch syndrome|Hereditary nonpolyposis colorectal neoplasms|Hereditary cancer-predisposing syndrome|Turcot syndrome|Muir-Torré syndrome|Colorectal cancer, hereditary nonpolyposis, type 2|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.