Variant (rsID / SNP)

rs1778057

rs1778057 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DICER1. Location: chromosome 14, position 95,566,108. Clinical significance in the table: Benign.

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Reference-table entries

DICER1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:95566108
Cytoband: 14q32.13
HGVS: NM_177438.3(DICER1):c.4206+9G>T
Allele change: Silent

Associated conditions / phenotypes

DICER1 syndrome|Goiter, multinodular 1, with or without Sertoli-Leydig cell tumors

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.