Variant (rsID / SNP)

rs202026056

rs202026056 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,643,436. Clinical significance in the table: Likely benign.

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Reference-table entries

MSH2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:47643436
Cytoband: 2p21
HGVS: NM_000251.3(MSH2):c.944G>T (p.Gly315Val)
Allele change: Missense_G315V

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Lynch syndrome|Hereditary nonpolyposis colorectal neoplasms|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.