Variant (rsID / SNP)
rs63750489
rs63750489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,061,817. Clinical significance in the table: Pathogenic.
Reference-table entries
MLH1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:37061817
- Cytoband
- 3p22.2
- HGVS
- NM_000249.4(MLH1):c.901C>T (p.Gln301Ter)
- Allele change
- Silent
Associated conditions / phenotypes
Lynch syndrome|Hereditary nonpolyposis colorectal neoplasms|See cases
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.