Variant (rsID / SNP)

rs770904411

rs770904411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DICER1. Location: chromosome 14, position 95,571,588. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DICER1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Deletion
Chromosome / position: 14:95571588
Cytoband: 14q32.13
HGVS: NM_177438.3(DICER1):c.3094-8_3094-5del

Associated conditions / phenotypes

Pleuropulmonary blastoma|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.