Variant (rsID / SNP)

rs587782626

rs587782626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,067,123. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MLH1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:37067123
Cytoband: 3p22.2
HGVS: NM_000249.4(MLH1):c.1039-5T>C
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms|Colorectal cancer, hereditary nonpolyposis, type 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.