Variant (rsID / SNP)

rs145400590

rs145400590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,672,679. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MSH2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:47672679
Cytoband: 2p21
HGVS: NM_000251.3(MSH2):c.1277-8T>C
Allele change: Silent

Associated conditions / phenotypes

Hereditary nonpolyposis colorectal neoplasms|Hereditary cancer-predisposing syndrome|Lynch syndrome 1|Malignant tumor of breast

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.