Variant (rsID / SNP)

rs139977567

rs139977567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUTYH. Location: chromosome 1, position 45,799,074. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MUTYHBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:45799074
Cytoband: 1p34.1
HGVS: NM_001048174.2(MUTYH):c.264+11G>A
Allele change: Silent

Associated conditions / phenotypes

Familial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|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.