Variant (rsID / SNP)

rs894876691

rs894876691 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MLH1. Location: chromosome 3, position 37,090,439. Clinical significance in the table: Likely benign.

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Reference-table entries

MLH1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:37090439
Cytoband: 3p22.2
HGVS: NM_000249.4(MLH1):c.2034A>G (p.Lys678=)
Allele change: Synonymous_K337K

Associated conditions / phenotypes

Hereditary nonpolyposis colorectal neoplasms|Hereditary cancer-predisposing syndrome

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.