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Variant (rsID / SNP)

rs189015988

MSH2

rs189015988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,657,091. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MSH2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:47657091
Cytoband
2p21
HGVS
NM_000251.3(MSH2):c.1276+11A>G
Allele change
Silent

Associated conditions / phenotypes

Lynch syndrome 1|Hereditary cancer-predisposing syndrome|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.