Variant (rsID / SNP)

rs1800937

rs1800937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,025,764. Clinical significance in the table: Benign.

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Reference-table entries

MSH6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:48025764
Cytoband: 2p16.3
HGVS: NM_000179.3(MSH6):c.642C>T (p.Tyr214=)
Allele change: Nonsense_Y84X

Associated conditions / phenotypes

Lynch syndrome|Hereditary cancer-predisposing syndrome|Colorectal cancer, hereditary nonpolyposis, type 5|Hereditary nonpolyposis colorectal neoplasms|Carcinoma of colon

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.