Variant (rsID / SNP)

rs786204082

rs786204082 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH2. Location: chromosome 2, position 47,637,357. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

MSH2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:47637357
Cytoband: 2p21
HGVS: NM_000251.3(MSH2):c.491G>A (p.Gly164Glu)
Allele change: Missense_G164E

Associated conditions / phenotypes

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

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.