Variant (rsID / SNP)

rs201523588

rs201523588 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DICER1. Location: chromosome 14, position 95,570,176. Clinical significance in the table: Uncertain significance.

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Reference-table entries

DICER1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:95570176
Cytoband: 14q32.13
HGVS: NM_177438.3(DICER1):c.3557A>G (p.Asn1186Ser)
Allele change: Missense_N1186I

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.