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Variant (rsID / SNP)

rs773807182

MSH6

rs773807182 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,033,425. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MSH6Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
2:48033425
Cytoband
2p16.3
HGVS
NM_000179.3(MSH6):c.3729A>G (p.Thr1243=)
Allele change
Synonymous_T1113T

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary nonpolyposis colorectal neoplasms|Colorectal cancer, hereditary nonpolyposis, type 5

Public references

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