Variant (rsID / SNP)

rs374950566

rs374950566 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUTYH. Location: chromosome 1, position 45,797,887. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

MUTYHPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:45797887
Cytoband: 1p34.1
HGVS: NM_001048174.2(MUTYH):c.800C>T (p.Pro267Leu)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon|Breast carcinoma

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.