Variant (rsID / SNP)
rs35831931
rs35831931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,092,019. Clinical significance in the table: Benign.
Reference-table entries
MLH1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:37092019
- Cytoband
- 3p22.2
- HGVS
- NM_000249.4(MLH1):c.2146G>A (p.Val716Met)
- Allele change
- Missense_V375M
Associated conditions / phenotypes
Lynch syndrome|Hereditary cancer-predisposing syndrome|Colorectal cancer, hereditary nonpolyposis, type 2|Hereditary nonpolyposis colorectal neoplasms|Malignant tumor of breast|Breast and/or ovarian cancer|Muir-Torré syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.