Variant (rsID / SNP)
rs587778997
rs587778997 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,042,470. Clinical significance in the table: Pathogenic.
Reference-table entries
MLH1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 3:37042470
- Cytoband
- 3p22.2
- HGVS
- NM_000249.4(MLH1):c.232del (p.Glu78fs)
Associated conditions / phenotypes
Lynch syndrome|Hereditary nonpolyposis colorectal neoplasms
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.