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Variant (rsID / SNP)

rs115198722

MSH3

rs115198722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH3. Location: chromosome 5, position 80,063,896. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MSH3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:80063896
Cytoband
5q14.1
HGVS
NM_002439.5(MSH3):c.2041C>T (p.Pro681Ser)
Allele change
Missense_P681S

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Endometrial carcinoma|Familial adenomatous polyposis 4

Public references

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