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Variant (rsID / SNP)

rs1060502023

MSH2

rs1060502023 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,690,295. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

MSH2Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
2:47690295
Cytoband
2p21
HGVS
NM_000251.3(MSH2):c.1510+2T>C
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Lynch syndrome 1|Hereditary nonpolyposis colorectal neoplasms

Public references

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