Variant (rsID / SNP)

rs377767363

rs377767363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMAD4. Location: chromosome 18, position 48,603,060. Clinical significance in the table: Pathogenic.

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Reference-table entries

SMAD4Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 18:48603060
Cytoband: 18q21.2
HGVS: NM_005359.6(SMAD4):c.1361_1364del (p.Ala454fs)

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.