Variant (rsID / SNP)

rs116953461

rs116953461 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DDX10. Location: chromosome 11, position 108,586,617. Clinical significance in the table: Benign.

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Reference-table entries

DDX10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:108586617
Cytoband: 11q22.3
HGVS: NM_004398.4(DDX10):c.1334A>G (p.Glu445Gly)
Allele change: Missense_E445G

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.