Variant (rsID / SNP)

rs786203744

rs786203744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,702,258. 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: 2:47702258
Cytoband: 2p21
HGVS: NM_000251.3(MSH2):c.1854A>G (p.Pro618=)
Allele change: Synonymous_P618P

Associated conditions / phenotypes

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

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.