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Variant (rsID / SNP)

rs533553381

MSH2

rs533553381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,703,705. 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
2:47703705
Cytoband
2p21
HGVS
NM_000251.3(MSH2):c.2205C>T (p.Ile735=)
Allele change
Synonymous_I735I

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Lynch 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.