Variant (rsID / SNP)

rs587781618

rs587781618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMAD4. Location: chromosome 18, position 48,593,558. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

SMAD4Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 18:48593558
Cytoband: 18q21.2
HGVS: NM_005359.6(SMAD4):c.1308+1G>T
Allele change: Silent

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.