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Variant (rsID / SNP)

rs3136351

MSH6

rs3136351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH6. Location: chromosome 2, position 48,030,632. 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
2:48030632
Cytoband
2p16.3
HGVS
NM_000179.3(MSH6):c.3246G>T (p.Pro1082=)
Allele change
Synonymous_P952P

Associated conditions / phenotypes

Lynch syndrome 1|Hereditary cancer-predisposing syndrome|Colorectal cancer, hereditary nonpolyposis, type 5|Hereditary nonpolyposis colorectal neoplasms|Breast and/or ovarian cancer

Public references

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