Variant (rsID / SNP)

rs2424932

rs2424932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNMT3B. Location: chromosome 20, position 31,396,536. Clinical significance in the table: Benign.

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Reference-table entries

DNMT3BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:31396536
Cytoband: 20q11.21
HGVS: NM_006892.4(DNMT3B):c.*827A>G
Allele change: Silent

Associated conditions / phenotypes

Immunodeficiency-centromeric instability-facial anomalies syndrome 1

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.