Variant (rsID / SNP)

rs886037680

rs886037680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DICER1. Location: chromosome 14, position 95,582,028. Clinical significance in the table: Pathogenic.

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Reference-table entries

DICER1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 14:95582028
Cytoband: 14q32.13
HGVS: NM_177438.3(DICER1):c.1880_1883del (p.Ile627fs)

Associated conditions / phenotypes

DICER1 syndrome|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.