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Variant (rsID / SNP)

rs141163928

DICER1

rs141163928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DICER1. Location: chromosome 14, position 95,584,087. 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
single nucleotide variant
Chromosome / position
14:95584087
Cytoband
14q32.13
HGVS
NM_177438.3(DICER1):c.1381A>G (p.Ile461Val)
Allele change
Missense_I461V

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|DICER1 syndrome|Malignant tumor of breast

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.